ICD-9 Code 759.89
Other specified congenital anomalies
Not Valid for Submission
759.89 is a legacy non-billable code used to specify a medical diagnosis of other specified congenital anomalies. This code was replaced on September 30, 2015 by its ICD-10 equivalent.
ICD-9: | 759.89 |
Short Description: | Specfied cong anomal NEC |
Long Description: | Other specified congenital anomalies |
Convert 759.89 to ICD-10
The following crosswalk between ICD-9 to ICD-10 is based based on the General Equivalence Mappings (GEMS) information:
- E78.71 - Barth syndrome
- E78.72 - Smith-Lemli-Opitz syndrome
- Q87.2 - Congenital malformation syndromes predom involving limbs
- Q87.3 - Congenital malformation syndromes involving early overgrowth
- Q87.5 - Oth congenital malformation syndromes w oth skeletal changes
- Q87.81 - Alport syndrome
- Q87.89 - Oth congenital malformation syndromes, NEC
- Q89.8 - Other specified congenital malformations
Code Classification
-
Congenital anomalies (740–759)
-
Congenital anomalies (740-759)
- 759 Other and unspecified congenital anomalies
-
Congenital anomalies (740-759)
Information for Medical Professionals
Synonyms
- Aarskog syndrome
- Aase syndrome
- Abnormal fetal duplication
- Abnormal fetus
- Acardia
- Acardiac monster
- Acardiacus anceps
- Acephalobrachius
- Acephalocheiria
- Acephalorhachia
- Acephalothorax
- Acquired and/or congenital pulmonary valve atresia
- Acquired mucociliary clearance defect
- Adams-Oliver syndrome
- Agnathus
- Allemann's syndrome
- Alport syndrome-like hereditary nephritis
- Alstrom syndrome
- Anadidymus
- Andersen Tawil syndrome
- Angelman syndrome
- Arteriohepatic dysplasia
- Asymmetric crying face association
- Atretocephalus
- Autositic monster
- Bannayan syndrome
- Bardet-Biedl syndrome
- Beckwith-Wiedemann syndrome
- Biemond's syndrome
- Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency
- Blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type
- Blepharophimosis-mental retardation syndrome, Say-Barber-Biesecker-Young-Simpson type
- Borjeson-Forssman-Lehmann syndrome
- Brachydactyly syndrome type C
- Branchiooculofacial syndrome
- Cardio-acral-facial syndrome
- Cardio-facio-cutaneous syndrome
- Carpenter's syndrome
- Caudal dysplasia sequence
- Celosomial monster
- Cerebro-costo-mandibular syndrome
- Cerebrofacial dysplasia
- Cerebro-oculo-facio-skeletal syndrome
- Child syndrome
- Chimera
- Chronic infantile neurological, cutaneous and articular syndrome
- Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis
- Cleft palate lateral synechia syndrome
- Cockayne syndrome
- Coffin-Lowry syndrome
- Coffin-Siris syndrome
- Cohen syndrome
- Cole-Carpenter dysplasia
- Coloboma, heart malformation, choanal atresia, retardation of growth and development, genital abnormalities, and ear malformations association
- Congenital absence of heart structure
- Congenital anomaly of trunk
- Congenital cataracts, facial dysmorphism and neuropathy
- Congenital contractural arachnodactyly
- Congenital deafness with labyrinthine aplasia, microtia and microdontia
- Congenital iodine deficiency syndrome
- Congenital iodine deficiency syndrome - mixed type
- Congenital iodine deficiency syndrome - neurological type
- Congenital malformation syndromes with metabolic disturbances
- Congenital muscular hypertrophy-cerebral syndrome
- Congenital sequelae of disorders
- Congenital stenosis
- Congenital viral hepatitis
- Cranial duplication
- Craniofacial deafness hand syndrome
- Cranio-orbito-ocular dysraphia syndrome
- Cross syndrome
- Cryopyrin associated periodic syndrome
- Cryptodidymus
- Currarino triad
- Cutis gyrata syndrome of Beare and Stevenson
- Cyclopia
- Cyclops hypognathus
- Cylindrical embryo
- Danon disease
- De Lange syndrome
- Deafness-dystonia-optic neuronopathy syndrome
- Derencephalus
- Diaphragmatic hernia, abnormal face and distal limb anomalies
- Diaphragmatic hernia-exomphalos-hypertelorism syndrome
- Dipodia
- Double monster
- Duane-radial ray syndrome
- Duhamel's syndrome
- Dyggve-Melchior-Clausen syndrome
- Dysmorphic sialidosis, congenital form
- Ear, patella, short stature syndrome
- Ectopic fetus
- Epilepsy, ataxia, sensorineural deafness, and tubulopathy syndrome
- Epstein syndrome
- Escobar syndrome
- Ethmocephalus
- Exstrophy of cloaca sequence
- Facial milia, lobate tongue, lingual and labial frenula syndrome
- Facio-auriculo-vertebral spectrum
- Femoral hypoplasia - unusual facies syndrome
- Fetal aminopterin syndrome
- Fetal hydantoin syndrome
- Fetal methyl mercury syndrome
- Fetal trimethadione syndrome
- Fetal valproate syndrome
- Fetal warfarin syndrome
- FG syndrome
- First arch syndrome
- Floating-Harbor syndrome
- Frasier syndrome
- Freeman-Sheldon syndrome
- Frontometaphyseal dysplasia
- Gardner syndrome
- Geleophysic dysplasia
- Genitopatellar syndrome
- Geroderma osteodysplastica
- Gillespie syndrome
- Gorlin-Chaudhry-Moss syndrome
- Grebe syndrome
- Grob's syndrome
- Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death
- Hand-foot-genital syndrome
- Hanhart's syndrome
- Hecht syndrome
- Hemihypertrophy of muscle
- Hereditary nephritis
- Holoacardius acephalus
- Holoacardius acormus
- Holoacardius amorphus
- Holt-Oram syndrome
- Homologous chimera
- Hyperhidrosis, premature cavities and premolar aplasia
- Hyperthermia-induced defect
- Hypogonadism, diabetes mellitus, alopecia, mental retardation and electrocardiographic abnormalities
- Ileoumbilical fistula
- Immotile cilia syndrome due to defective radial spokes
- Immotile cilia syndrome due to excessively long cilia
- Immunodeficiency associated with multiple organ system abnormalities
- Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
- Intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomaly syndrome
- Iris coloboma with ptosis, hypertelorism, and mental retardation
- Isologous chimera
- Johanson-Blizzard syndrome
- Kenny syndrome
- Klippel-Trenaunay-Weber syndrome
- Knuckle pads, deafness AND leukonychia syndrome
- Laminar heterotopia
- Langer-Giedion syndrome
- Larsen syndrome
- Laterality sequence
- Lenz microphthalmia syndrome
- Lethal Kniest-like syndrome
- Lethal multiple pterygium syndrome
- Levy-Hollister syndrome
- Limb reduction-ichthyosis syndrome
- Loeys-Dietz syndrome
- Lymphopenic agammaglobulinemia - short-limbed dwarfism syndrome
- Macrocephaly-capillary malformation
- Manitoba oculotrichoanal syndrome
- Marchesani syndrome
- Marden Walker syndrome
- Marfanoid joint hypermobility syndrome
- Marshall syndrome
- Marshall-Smith syndrome
- Maternal phenylketonuria fetal effect
- Meckel-Gruber syndrome
- Megalencephaly-capillary malformation syndrome
- Melnick-Fraser syndrome
- Menkes kinky-hair syndrome
- Mental retardation, dwarfism, and gonadal hypoplasia due to xeroderma pigmentosa
- Mermaid sirenomelia
- Microcephaly-capillary malformation syndrome
- Microcephaly-oculo-digito-esophageal-duodenal syndrome
- Midline facial cleft - Tessier cleft 30
- Mietens syndrome
- Miller syndrome
- Mohr syndrome
- Monocephalus tetrapus dibrachius
- Monster
- Monster with cranial anomalies
- Moore-Federman syndrome
- Mowat-Wilson syndrome
- Mulibrey nanism syndrome
- Multiple malformation syndrome due to non-infectious environmental agents
- Multiple malformation syndrome with early overgrowth
- Multiple malformation syndrome with facial defects as major feature
- Multiple malformation syndrome with facial-limb defects as major feature
- Multiple malformation syndrome with limb defect as major feature
- Multiple malformation syndrome with senile-like appearance
- Multiple malformation syndrome with unusual brain and/or neuromuscular findings
- Multiple malformation syndrome, moderate short stature, facial
- Multiple malformation syndrome, small stature, without skeletal dysplasia
- MVRCS association
- Myhre syndrome
- Nail-patella syndrome
- Nance-Horan syndrome
- Neu-Laxova syndrome
- Neurocutaneous syndrome
- Nodular embryo
- Noonan's syndrome
- Oculo-cerebro-cutaneous syndrome
- Oculodental syndrome
- Oculodentodigital syndrome
- Oculodento-osseous dysplasia
- Oculodento-osseous dysplasia - mild type
- Oculodento-osseous dysplasia - severe type
- Oculofaciocardiodental syndrome
- Oculo-palato-digital syndrome
- Oculoskeletal dysplasia
- Oral-facial-digital syndrome
- Oromandibular-limb hypogenesis spectrum
- Osteochondrodysplasia with osteopetrosis
- Otocephalic syndrome
- Oto-onycho-peroneal syndrome
- Oto-palato-digital syndrome, type I
- Oto-palato-digital syndrome, type II
- Otospondylomegaepiphyseal dysplasia
- Pallister-Hall syndrome
- Papillon-Lefèvre syndrome
- Parasitic monster
- Patent ductus arteriosus with facial dysmorphism and abnormal fifth digits
- Pena-Shokeir phenotype
- Pentalogy of Cantrell
- Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome
- Pili torti-deafness syndrome
- Podencephalus
- Polysomatous monster
- Port-wine stain in Rubinstein-Taybi syndrome
- Posterior fossa brain malformation, haemaniogma, arterial anomaly, cardiac defect and aortic coarctation, eye abnormality synodrome and sternal anomaly syndrome
- Posterior fossa brain malformation, hemangioma, arterial anomaly, cardiac defect and aortic coarctation, and eye abnormality syndrome
- Progeroid short stature with pigmented nevi
- Progressive hereditary glomerulonephritis without deafness
- Proteus syndrome
- Radial aplasia-thrombocytopenia syndrome
- Radiation chimera
- RAPADILINO syndrome
- Renal coloboma syndrome
- Renal dysplasia and retinal aplasia
- Renpenning syndrome
- Retinal detachment and occipital encephalocele
- Retinoic acid embryopathy
- Robinow syndrome
- Robinson nail dystrophy-deafness syndrome
- Rothmund-Thomson syndrome
- Royer's syndrome
- Rubinstein-Taybi syndrome
- Rud's syndrome
- Russell-Silver syndrome
- Rutland ciliary disorientation syndrome
- Ruvalcaba syndrome
- Ruvalcaba-Myhre syndrome
- Saldino-Mainzer dysplasia
- Schinzel-Giedion syndrome
- Schwartz syndrome
- Schwartz-Jampel syndrome
- Seckel syndrome
- Secondary ciliary dyskinesia
- Senter syndrome
- Shprintzen syndrome
- Simpson-Golabi-Behmel syndrome
- Single monster
- Sirenoform monster
- Sirenomelia sequence
- Smith-Lemli-Opitz syndrome
- Spondyloenchondrodysplasia with immune dysregulation
- Stickler syndrome
- Stunted embryo
- Suspect cystic fibrosis fetus
- Symphalangism-brachydactyly syndrome
- Synotus
- Thalidomide embryopathy syndrome
- Thoracoceloschisis
- Timothy syndrome type 1
- Townes syndrome
- Transient mucociliary clearance defect
- Tricho-dento-osseous syndrome
- Trichohepatoenteric syndrome
- Trichorhinophalangeal dysplasia type I
- Trichorhinophalangeal syndrome
- Tricho-thiodystrophy
- Triplet monster
- Type III short rib polydactyly syndrome
- Ulnar mammary syndrome
- Umbilical fistula
- Venous-lymphatic malformation
- Vertebral abnormalities, anal atresia, cardiac abnormalities, tracheo-esophageal fistula, limb defects syndrome
- Vertebral anomalies/dysgenesis, anal atresia, tracheo-esophageal fistula, esophageal atresia, renal anomalies, radial dysplasia association
- Warburg syndrome
- Warsaw breakage syndrome
- Weaver syndrome
- Weill-Marchesani syndrome
- Wildervanck's syndrome
- Williams syndrome
- Wissler-Fanconi syndrome
- X-linked mental retardation syndrome, Christianson type
- Young's syndrome
- Zimmermann-Laband syndrome
Index to Diseases and Injuries
References found for the code 759.89 in the Index of Diseases and Injuries:
- Abrachiocephalia 759.89
- Abrachiocephalus 759.89
- Absence organ or part complete or partial
- heart congenital 759.89
- acquired see Status organ replacement
- heart congenital 759.89
- Acardia 759.89
- Arcadiacus amorphus 759.89
- Acardius 759.89
- Acephalobrachia 759.89
- Acephalocardia 759.89
- Acephalocardius 759.89
- Acephalochiria 759.89
- Acephalochirus 759.89
- Acephalogaster 759.89
- Acephalostomus 759.89
- Acephalothorax 759.89
- Alagille syndrome 759.89
- Alport s syndrome hereditary hematurianephropathy deafness 759.89
- Anomaly anomalous congenital unspecified type 759.9
- organ
- specified type NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular.
- Atresia atretic congenital 759.89
- alimentary organ or tract NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 751.8- lower 751.2
- upper 750.8
- ani anus anal canal 751.2
- aorta 747.22
- with hypoplasia of ascending aorta and defective development of left ventricle with mitral valve atresia 746.7
- arch 747.11
- ring 747.21
- aortic orifice valve 746.89
- arch 747.11
- aqueduct of Sylvius 742.3
- with spina bifida SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Spina bifida 741.0
- with spina bifida SEE ALSO See Also
- artery NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Atresia blood vessel 747.60- cerebral 747.81
- coronary 746.85
- eye 743.58
- pulmonary 747.31
- umbilical 747.5
- auditory canal external 744.02
- bile biliary duct common or passage 751.61
- acquired SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Obstruction biliary 576.2
- acquired SEE ALSO See Also
- blood vessel peripheral NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 747.60- cerebral 747.81
- gastrointestinal 747.61
- lower limb 747.64
- pulmonary artery 747.31
- renal 747.62
- spinal 747.82
- upper limb 747.63
- bronchus 748.3
- canal ear 744.02
- cardiac
- valve 746.89
- aortic 746.89
- mitral 746.89
- pulmonary 746.01
- tricuspid 746.1
- valve 746.89
- cecum 751.2
- cervix acquired 622.4
- congenital 752.43
- in pregnancy or childbirth 654.6
- affecting fetus or newborn 763.89
- causing obstructed labor 660.2
- affecting fetus or newborn 763.1
- choana 748.0
- colon 751.2
- cystic duct 751.61
- acquired 575.8
- with obstruction SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Obstruction gallbladder 575.2
- with obstruction SEE ALSO See Also
- acquired 575.8
- digestive organs NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 751.8
- duodenum 751.1
- ear canal 744.02
- ejaculatory duct 752.89
- epiglottis 748.3
- esophagus 750.3
- Eustachian tube 744.24
- fallopian tube acquired 628.2
- congenital 752.19
- follicular cyst 620.0
- foramen of
- Luschka 742.3
- with spina bifida SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Spina bifida 741.0
- with spina bifida SEE ALSO See Also
- Magendie 742.3
- with spina bifida SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Spina bifida 741.0
- with spina bifida SEE ALSO See Also
- Luschka 742.3
- gallbladder 751.69
- genital organ
- external
- female 752.49
- internal
- female 752.89
- male 752.89
- external
- glottis 748.3
- gullet 750.3
- heart
- valve NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 746.89- aortic 746.89
- mitral 746.89
- pulmonary 746.01
- tricuspid 746.1
- valve NEC NEC "Not elsewhere classifiable"
- hymen 752.42
- acquired 623.3
- postinfective 623.3
- ileum 751.1
- intestine small 751.1
- large 751.2
- iris filtration angle SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Buphthalmia 743.20
- jejunum 751.1
- kidney 753.3
- lacrimal apparatus 743.65
- acquired see Stenosis lacrimal
- larynx 748.3
- ligament broad 752.19
- lung 748.5
- meatus urinarius 753.6
- mitral valve 746.89
- with atresia or hypoplasia of aortic orifice or valve with hypoplasia of ascending aorta and defective development of left ventricle 746.7
- nares anterior posterior 748.0
- nasolacrimal duct 743.65
- nasopharynx 748.8
- nose nostril 748.0
- acquired 738.0
- organ or site NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. see Anomaly specified type NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular.
- osseous meatus ear 744.03
- oviduct acquired 628.2
- congenital 752.19
- parotid duct 750.23
- acquired 527.8
- pulmonary artery 747.31
- valve 746.01
- vein 747.49
- pulmonic 746.01
- pupil 743.46
- rectum 751.2
- salivary duct or gland 750.23
- acquired 527.8
- sublingual duct 750.23
- acquired 527.8
- submaxillary duct or gland 750.23
- acquired 527.8
- trachea 748.3
- tricuspid valve 746.1
- ureter 753.29
- ureteropelvic junction 753.21
- ureterovesical orifice 753.22
- urethra valvular 753.6
- urinary tract NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 753.29
- uterus 752.31
- acquired 621.8
- vagina acquired 623.2
- congenital total partial 752.45
- postgonococcal old 098.2
- postinfectional 623.2
- senile 623.2
- vascular NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Atresia blood vessel 747.60- cerebral 747.81
- vas deferens 752.89
- vein NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Atresia blood vessel 747.60- cardiac 746.89
- great 747.49
- portal 747.49
- pulmonary 747.49
- vena cava inferior superior 747.49
- vesicourethral orifice 753.6
- vulva 752.49
- acquired 624.8
- alimentary organ or tract NEC NEC "Not elsewhere classifiable"
- Barth syndrome 759.89
- Beckwith Wiedemann syndrome 759.89
- Biedl Bardet syndrome 759.89
- Biemond s syndrome obesity polydactyly and intellectual disabilities 759.89
- Birt Hogg Dube syndrome 759.89
- Brachman de Lange syndrome Amsterdam dwarf intellectual disabilities and brachycephaly 759.89
- Brachymorphism and ectopia lentis 759.89
- Bruck de Lange disease or syndrome Amsterdam dwarf intellectual disabilities and brachycephaly 759.89
- Carpenter s syndrome 759.89
- Cerebrohepatorenal syndrome 759.89
- CGF congenital generalized fibromatosis 759.89
- CHARGE association syndrome 759.89
- Cockayne s disease or syndrome microcephaly and dwarfism 759.89
- Congenital SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. condition- generalized fibromatosis CGF 759.89
- Cornelia de Lange s syndrome Amsterdam dwarf intellectual disabilities and brachycephaly 759.89
- Cyclencephaly 759.89
- Cyclopia cyclops 759.89
- Cyllosoma 759.89
- Cyst mucus retention serous simple
- congenital NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 759.89- adrenal glands 759.1
- epiglottis 748.3
- esophagus 750.4
- fallopian tube 752.11
- kidney 753.10
- multiple 753.19
- single 753.11
- larynx 748.3
- liver 751.62
- lung 748.4
- mediastinum 748.8
- ovary 752.0
- oviduct 752.11
- pancreas 751.7
- periurethral tissue 753.8
- prepuce NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 752.69- penis 752.69
- sublingual 750.26
- submaxillary gland 750.26
- thymus gland 759.2
- tongue 750.19
- ureterovesical orifice 753.4
- vulva 752.41
- umbilicus 759.89
- congenital NEC NEC "Not elsewhere classifiable"
- Deformity 738.9
- de Lange s syndrome Amsterdam dwarf intellectual disabilities and brachycephaly 759.89
- Disease diseased SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Syndrome- Bruck de Lange Amsterdam dwarf intellectual disabilities and brachycephaly 759.89
- Cockayne s microcephaly and dwarfism 759.89
- Kok 759.89
- lymphoproliferative chronic M9970 1 238.79
- X linked 759.89
- polycystic congenital 759.89
- kidney or renal 753.12
- adult type APKD 753.13
- autosomal dominant 753.13
- autosomal recessive 753.14
- childhood type CPKD 753.14
- infantile type 753.14
- liver or hepatic 751.62
- lung or pulmonary 518.89
- congenital 748.4
- ovary ovaries 256.4
- spleen 759.0
- kidney or renal 753.12
- Startle 759.89
- Dwarf dwarfism 259.4
- Amsterdam 759.89
- bird headed 759.89
- Russell s uterine dwarfism and craniofacial dysostosis 759.89
- Dyscraniopyophalangy 759.89
- Dysostosis
- orodigitofacial 759.89
- Dysplasia SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Anomaly- craniocarpotarsal 759.89
- linguofacialis 759.89
- oculodentodigital 759.89
- Ectopic ectopia congenital 759.89
- abdominal viscera 751.8
- due to defect in anterior abdominal wall 756.79
- ACTH syndrome 255.0
- adrenal gland 759.1
- anus 751.5
- auricular beats 427.61
- beats 427.60
- bladder 753.5
- bone and cartilage in lung 748.69
- brain 742.4
- breast tissue 757.6
- cardiac 746.87
- cerebral 742.4
- cordis 746.87
- endometrium 617.9
- gallbladder 751.69
- gastric mucosa 750.7
- gestation see Pregnancy ectopic
- heart 746.87
- hormone secretion NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 259.3
- hyperparathyroidism 259.3
- kidney crossed intrathoracic pelvis 753.3
- in pregnancy or childbirth 654.4
- causing obstructed labor 660.2
- in pregnancy or childbirth 654.4
- lens 743.37
- lentis 743.37
- mole see Pregnancy ectopic
- organ or site NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. see Malposition congenital
- ovary 752.0
- pancreas pancreatic tissue 751.7
- pregnancy see Pregnancy ectopic
- pupil 364.75
- renal 753.3
- sebaceous glands of mouth 750.26
- secretion
- ACTH 255.0
- adrenal hormone 259.3
- adrenalin 259.3
- adrenocorticotropin 255.0
- antidiuretic hormone ADH 259.3
- epinephrine 259.3
- norepinephrine 259.3
- pituitary posterior 259.3
- spleen 759.0
- testis 752.51
- thyroid 759.2
- ureter 753.4
- ventricular beats 427.69
- vesicae 753.5
- abdominal viscera 751.8
- Fibromatosis 728.79
- congenital generalized CGF 759.89
- Finnish type nephrosis congenital 759.89
- Fistula sinus 686.9
- umbilical 759.89
- Fraser s syndrome 759.89
- Freeman Sheldon syndrome 759.89
- Gillespie s syndrome dysplasia oculodentodigitalis 759.89
- Glaucoma capsular inflammatory noninflammatory primary 365.9
- Gorlin Chaudhry Moss syndrome 759.89
- Hemihypertrophy congenital 759.89
- cranial 756.0
- Hyperekplexia 759.89
- Hyperexplexia 759.89
- Hypoplasia hypoplasis 759.89
- adrenal gland 759.1
- alimentary tract 751.8
- lower 751.2
- upper 750.8
- angiolymphoid with eosinophilia ALHE 228.01
- anus anal canal 751.2
- aorta 747.22
- aortic
- arch tubular 747.10
- orifice or valve with hypoplasia of ascending aorta and defective development of left ventricle with mitral valve atresia 746.7
- appendix 751.2
- areola 757.6
- arm SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence arm congenital 755.20
- artery congenital peripheral 747.60
- brain 747.81
- cerebral 747.81
- coronary 746.85
- gastrointestinal 747.61
- lower limb 747.64
- pulmonary 747.31
- renal 747.62
- retinal 743.58
- spinal 747.82
- umbilical 747.5
- upper limb 747.63
- auditory canal 744.29
- causing impairment of hearing 744.02
- biliary duct common or passage 751.61
- bladder 753.8
- bone NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 756.9- face 756.0
- malar 756.0
- mandible 524.04
- alveolar 524.74
- marrow 284.9
- acquired secondary 284.89
- congenital 284.09
- idiopathic 284.9
- maxilla 524.03
- alveolar 524.73
- skull SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Hypoplasia skull 756.0
- brain 742.1
- gyri 742.2
- specified part 742.2
- breast areola 611.82
- bronchus tree 748.3
- cardiac 746.89
- valve see Hypoplasia heart valve
- vein 746.89
- carpus SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence carpal congenital 755.28
- cartilaginous 756.9
- cecum 751.2
- cementum 520.4
- hereditary 520.5
- cephalic 742.1
- cerebellum 742.2
- cervix uteri 752.43
- chin 524.06
- clavicle 755.51
- coccyx 756.19
- colon 751.2
- corpus callosum 742.2
- cricoid cartilage 748.3
- dermal focal Goltz 757.39
- digestive organ s or tract NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 751.8- lower 751.2
- upper 750.8
- ear 744.29
- auricle 744.23
- lobe 744.29
- middle except ossicles 744.03
- ossicles 744.04
- ossicles 744.04
- enamel of teeth neonatal postnatal prenatal 520.4
- hereditary 520.5
- endocrine gland NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 759.2
- endometrium 621.8
- epididymis 752.89
- epiglottis 748.3
- erythroid congenital 284.01
- erythropoietic chronic acquired 284.81
- esophagus 750.3
- Eustachian tube 744.24
- eye SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Microphthalmos 743.10- lid 743.62
- face 744.89
- bone s 756.0
- fallopian tube 752.19
- femur SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence femur congenital 755.34
- fibula SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence fibula congenital 755.37
- finger SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence finger congenital 755.29
- focal dermal 757.39
- foot 755.31
- gallbladder 751.69
- genitalia genital organ s
- female 752.89
- external 752.49
- in adiposogenital dystrophy 253.8
- male 752.89
- penis 752.69
- female 752.89
- glottis 748.3
- hair 757.4
- hand 755.21
- heart 746.89
- left complex syndrome 746.7
- humerus SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence humerus congenital 755.24
- hymen 752.49
- intestine small 751.1
- large 751.2
- iris 743.46
- jaw 524.09
- kidney s 753.0
- labium majus minus 752.49
- labyrinth membranous 744.05
- lacrimal duct apparatus 743.65
- larynx 748.3
- leg SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence limb congenital lower 755.30
- limb 755.4
- lower SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence limb congenital lower 755.30
- upper SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence limb congenital upper 755.20
- lower SEE ALSO See Also
- liver 751.69
- lung lobe 748.5
- mammary areolar 611.82
- mandibular 524.04
- alveolar 524.74
- unilateral condylar 526.89
- maxillary 524.03
- alveolar 524.73
- medullary 284.9
- megakaryocytic 287.30
- metacarpus SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence metacarpal congenital 755.28
- metatarsus SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence metatarsal congenital 755.38
- muscle 756.89
- eye 743.69
- myocardium congenital Uhl s anomaly 746.84
- nail s 757.5
- nasolacrimal duct 743.65
- nervous system NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 742.8
- neural 742.8
- nose nasal 748.1
- ophthalmic SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Microphthalmos 743.10
- optic nerve 377.43
- organ
- of Corti 744.05
- osseous meatus ear 744.03
- ovary 752.0
- oviduct 752.19
- pancreas 751.7
- parathyroid gland 759.2
- parotid gland 750.26
- patella 755.64
- pelvis pelvic girdle 755.69
- penis 752.69
- peripheral vascular system congenital NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 747.60- gastrointestinal 747.61
- lower limb 747.64
- renal 747.62
- spinal 747.82
- upper limb 747.63
- pituitary gland 759.2
- pulmonary 748.5
- arteriovenous 747.32
- artery 747.31
- valve 746.01
- punctum lacrimale 743.65
- radioulnar SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence radius congenital with ulna 755.25
- radius SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence radius congenital 755.26
- rectum 751.2
- respiratory system NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. 748.9
- rib 756.3
- sacrum 756.19
- scapula 755.59
- shoulder girdle 755.59
- skin 757.39
- skull bone 756.0
- with
- anencephalus 740.0
- encephalocele 742.0
- hydrocephalus 742.3
- with spina bifida SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Spina bifida 741.0
- with spina bifida SEE ALSO See Also
- microcephalus 742.1
- with
- spinal cord ventral horn cell 742.59
- vessel 747.82
- spine 756.19
- spleen 759.0
- sternum 756.3
- tarsus SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence tarsal congenital 755.38
- testis testicle 752.89
- thymus gland 279.11
- thyroid gland 243
- cartilage 748.3
- tibiofibular SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence tibia congenital with fibula 755.35
- toe SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence toe congenital 755.39
- tongue 750.16
- trachea cartilage rings 748.3
- Turner s tooth 520.4
- ulna SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Absence ulna congenital 755.27
- umbilical artery 747.5
- ureter 753.29
- uterus 752.32
- vagina 752.45
- vascular peripheral NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Hypoplasia peripheral vascular system 747.60- brain 747.81
- vein s peripheral NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Hypoplasia peripheral vascular system 747.60- brain 747.81
- cardiac 746.89
- great 747.49
- portal 747.49
- pulmonary 747.49
- vena cava inferior superior 747.49
- vertebra 756.19
- vulva 752.49
- zonule ciliary 743.39
- zygoma 738.12
- Joubert syndrome 759.89
- Kabuki syndrome 759.89
- Klippel Trenaunay syndrome 759.89
- Laurence Moon Biedl syndrome obesity polydactyly and intellectual disabilities 759.89
- Marchesani Weill syndrome brachymorphism and ectopia lentis 759.89
- Meyer Schwickerath and Weyers syndrome dysplasia oculodentodigitalis 759.89
- Microphthalmos congenital 743.10
- syndrome 759.89
- Mieten s syndrome 759.89
- Mohr s syndrome types I and II 759.89
- Myofibromatosis
- infantile 759.89
- Negri bodies 071
- Neill Dingwall syndrome microcephaly and dwarfism 759.89
- Nephritis nephritic albuminuric azotemic congenital degenerative diffuse disseminated epithelial familial focal granulomatous hemorrhagic infantile nonsuppurative excretory uremic 583.9
- hereditary Alport s syndrome 759.89
- Nephrosis nephrotic Epstein s syndrome 581.9
- Finnish type congenital 759.89
- Nevus M8720 0 SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Neoplasm skin benign- flammeus 757.32
- osteohypertrophic 759.89
- osteohypertrophic flammeus 759.89
- flammeus 757.32
- Orodigitofacial dysostosis 759.89
- Papillon L age and Psaume syndrome orodigitofacial dysostosis 759.89
- Persistence persistent congenital 759.89
- anal membrane 751.2
- arteria stapedia 744.04
- atrioventricular canal 745.69
- bloody ejaculate 792.2
- branchial cleft 744.41
- bulbus cordis in left ventricle 745.8
- canal of Cloquet 743.51
- capsule opaque 743.51
- cilioretinal artery or vein 743.51
- cloaca 751.5
- communication see Fistula congenital
- convolutions
- aortic arch 747.21
- fallopian tube 752.19
- oviduct 752.19
- uterine tube 752.19
- double aortic arch 747.21
- ductus
- arteriosus 747.0
- Botalli 747.0
- fetal
- circulation 747.83
- form of cervix uteri 752.49
- hemoglobin hereditary quot Swiss variety quot 282.7
- pulmonary hypertension 747.83
- foramen
- Botalli 745.5
- ovale 745.5
- Gartner s duct 752.41
- hemoglobin fetal hereditary HPFH 282.7
- hyaloid
- artery generally incomplete 743.51
- system 743.51
- hymen tag
- in pregnancy or childbirth 654.8
- causing obstructed labor 660.2
- in pregnancy or childbirth 654.8
- lanugo 757.4
- left
- posterior cardinal vein 747.49
- root with right arch of aorta 747.21
- superior vena cava 747.49
- Meckel s diverticulum 751.0
- mesonephric duct 752.89
- fallopian tube 752.11
- mucosal disease middle ear with posterior or superior marginal perforation of ear drum 382.2
- nail s anomalous 757.5
- occiput anterior or posterior 660.3
- fetus or newborn 763.1
- omphalomesenteric duct 751.0
- organ or site NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular. see Anomaly specified type NEC NEC "Not elsewhere classifiable"
This abbreviation in the index represents “other specified” when a specific code is not available for a condition the index directs the coder to the “other specified” code in the tabular.
- ostium
- atrioventriculare commune 745.69
- primum 745.61
- secundum 745.5
- ovarian rests in fallopian tube 752.19
- pancreatic tissue in intestinal tract 751.5
- primary deciduous
- teeth 520.6
- vitreous hyperplasia 743.51
- pulmonary hypertension 747.83
- pupillary membrane 743.46
- iris 743.46
- Rhesus Rh titer SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Complications transfusion 999.70
- right aortic arch 747.21
- sinus
- urogenitalis 752.89
- venosus with imperfect incorporation in right auricle 747.49
- thymus gland 254.8
- hyperplasia 254.0
- thyroglossal duct 759.2
- thyrolingual duct 759.2
- truncus arteriosus or communis 745.0
- tunica vasculosa lentis 743.39
- umbilical sinus 753.7
- urachus 753.7
- vegetative state 780.03
- vitelline duct 751.0
- wolffian duct 752.89
- Podencephalus 759.89
- Polycystic congenital disease 759.89
- degeneration kidney see Polycystic kidney
- kidney congenital 753.12
- adult type APKD 753.13
- autosomal dominant 753.13
- autosomal recessive 753.14
- childhood type CPKD 753.14
- infantile type 753.14
- liver 751.62
- lung 518.89
- congenital 748.4
- ovary ovaries 256.4
- spleen 759.0
- Pseudo Turner s syndrome 759.89
- Rubinstein Taybi s syndrome brachydactylia short stature and intellectual disabilities 759.89
- Rud s syndrome mental deficiency epilepsy and infantilism 759.89
- Russell s dwarf uterine dwarfism and craniofacial dysostosis 759.89
- Russell Silver syndrome congenital hemihypertrophy and short stature 759.89
- Seborrhea seborrheic 706.3
- nigricans 759.89
- Seckel s syndrome 759.89
- Sick 799.9
- cilia syndrome 759.89
- Silver s syndrome congenital hemihypertrophy and short stature 759.89
- Sirenomelia 759.89
- Smith Lemli Opitz syndrome cerebrohepatorenal syndrome 759.89
- Stickler syndrome 759.89
- Stiff baby 759.89
- Sympus 759.89
- Syndrome SEE ALSO See Also
A “see also” instruction following a main term in the index instructs that there is another main term that may also be referenced that may provide additional index entries that may be useful. It is not necessary to follow the “see also” note when the original main term provides the necessary code. Disease- Alagille 759.89
- Alport s hereditary hematuria nephropathy deafness 759.89
- Angelman 759.89
- Bardet Biedl obesity polydactyly and intellectual disabilities 759.89
- Barth 759.89
- basal cell nevus 759.89
- Beckwith Wiedemann 759.89
- Biedl Bardet obesity polydactyly and intellectual disabilities 759.89
- Biemond s obesity polydactyly and intellectual disabilities 759.89
- Birt Hogg Dube 759.89
- Borjeson Forssman Lehmann 759.89
- Brachman de Lange Amsterdam dwarf intellectual disabilities and brachycephaly 759.89
- cardiofaciocutaneous 759.89
- Carpenter s 759.89
- cerebrohepatorenal 759.89
- CHARGE association 759.89
- Cockayne s microencephaly and dwarfism 759.89
- Coffin Lowry 759.89
- congenital
- affecting more than one system 759.7
- muscular hypertrophy cerebral 759.89
- de Lange s Amsterdam dwarf intellectual disabilities and brachycephaly Cornelia 759.89
- Fraser s 759.89
- Freeman Sheldon 759.89
- Gillespie s dysplasia oculodentodigitalis 759.89
- Gorlin Chaudhry Moss 759.89
- Gorlin s 759.89
- inverted Marfan s 759.89
- Joubert 759.89
- Kabuki 759.89
- Klippel Trenaunay 759.89
- Laurence Moon Bardet Biedl obesity polydactyly and intellectual disabilities 759.89
- Marchesani Weill brachymorphism and ectopia lentis 759.89
- Menkes 759.89
- glutamic acid 759.89
- maple syrup urine disease 270.3
- Meyer Schwickerath and Weyers dysplasia oculodentodigitalis 759.89
- microphthalmos congenital 759.89
- Mieten s 759.89
- Mohr s types I and II 759.89
- Neill Dingwall microencephaly and dwarfism 759.89
- Noonan s 759.89
- oral facial digital 759.89
- ordigitofacial 759.89
- otopalatodigital 759.89
- Papillon L age and Psaume orodigitofacial dysostosis 759.89
- pseudo Turner s 759.89
- Rubinstein Taybi s brachydactylia short stature and intellectual disabilities 759.89
- Rud s mental deficiency epilepsy and infantilism 759.89
- Russell Silver congenital hemihypertrophy and short stature 759.89
- Seckel s 759.89
- sick
- cilia 759.89
- Silver s congenital hemihypertrophy and short stature 759.89
- Smith Lemli Opitz cerebrohepatorenal syndrome 759.89
- spherophakia brachymorphia 759.89
- Stickler 759.89
- stiff baby 759.89
- Taybi s otopalatodigital 759.89
- Ullrich Feichtiger 759.89
- VATER 759.89
- Weill Marchesani brachymorphism and ectopia lentis 759.89
- quot whistling face quot craniocarpotarsal dystrophy 759.89
- Synophthalmus 759.89
- Taybi s syndrome otopalatodigital 759.89
- Teratencephalus 759.89
- Thoracogastroschisis congenital 759.89
- Ullrich Feichtiger syndrome 759.89
- VATER syndrome 759.89
- Weill Marchesani syndrome brachymorphism and ectopia lentis 759.89
- quot Whistling face quot syndrome craniocarpotarsal dystrophy 759.89
Information for Patients
Birth Defects
What are birth defects?
A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the first 3 months of pregnancy. One out of every 33 babies in the United States is born with a birth defect.
A birth defect may affect how the body looks, works, or both. Some birth defects like cleft lip or neural tube defects are structural problems that can be easy to see. Others, like heart disease, are found using special tests. Birth defects can range from mild to severe. How a birth defect affects a child's life depends mostly on which organ or body part is involved and how severe the defect is.
What causes birth defects?
For some birth defects, researchers know the cause. But for many birth defects, the exact cause is unknown. Researchers think that most birth defects are caused by a complex mix of factors, which can include:
- Genetics. One or more genes might have a change or mutation that prevents them from working properly. For example, this happens in Fragile X syndrome. With some defects, a gene or part of the gene might be missing.
- Chromosomal problems. In some cases, a chromosome or part of a chromosome might be missing. This is what happens in Turner syndrome. In other cases, such as with Down syndrome, the child has an extra chromosome.
- Exposures to medicines, chemicals, or other toxic substances. For example, alcohol misuse can cause fetal alcohol spectrum disorders.
- Infections during pregnancy. For example, infection with Zika virus during pregnancy can cause a serious defect in the brain.
- Lack of certain nutrients. Not getting enough folic acid before and during pregnancy is a key factor in causing neural tube defects.
Who is at risk of having a baby with birth defects?
Certain factors may might increase the chances of having a baby with a birth defect, such as:
- Smoking, drinking alcohol, or taking certain "street" drugs during pregnancy
- Having certain medical conditions, such as obesity or uncontrolled diabetes, before and during pregnancy
- Taking certain medicines
- Having someone in your family with a birth defect. To learn more about your risk of having a baby with a birth defect, you can talk with a genetic counselor,
- Being an older mother, typically over the age of 34 years
How are birth defects diagnosed?
Health care providers can diagnose some birth defects during pregnancy, using prenatal testing. That's why it important to get regular prenatal care.
Other birth defects may not be found until after the baby is born. Providers may find them through newborn screening. Some defects, such as club foot, are obvious right away. Other times, the health care provider may not discover a defect until later in life, when the child has symptoms.
What are the treatments for birth defects?
Children with birth defects often need special care and treatments. Because the symptoms and problems caused by birth defects vary, the treatments also vary. Possible treatments may include surgery, medicines, assistive devices, physical therapy, and speech therapy.
Often, children with birth defects need a variety of services and may need to see several specialists. The primary health care provider can coordinate the special care that the child needs.
Can birth defects be prevented?
Not all birth defects can be prevented. But there are things you can do before and during pregnancy to increase your chance of having a healthy baby:
- Start prenatal care as soon as you think you might be pregnant, and see your health care provider regularly during pregnancy
- Get 400 micrograms (mcg) of folic acid every day. If possible, you should start taking it at least one month before you get pregnant.
- Don't drink alcohol, smoke, or use "street" drugs
- Talk to your health care provider about any medicines you are taking or thinking about taking. This includes prescription and over-the-counter medicines, as well as dietary or herbal supplements.
- Learn how to prevent infections during pregnancy
- If you have any medical conditions, try to get them under control before you get pregnant
Centers for Disease Control and Prevention
[Read More]
ICD-9 Footnotes
General Equivalence Map Definitions
The ICD-9 and ICD-10 GEMs are used to facilitate linking between the diagnosis codes in ICD-9-CM and the new ICD-10-CM code set. The GEMs are the raw material from which providers, health information vendors and payers can derive specific applied mappings to meet their needs.
- Approximate Flag - The approximate flag is on, indicating that the relationship between the code in the source system and the code in the target system is an approximate equivalent.
- No Map Flag - The no map flag indicates that a code in the source system is not linked to any code in the target system.
- Combination Flag - The combination flag indicates that more than one code in the target system is required to satisfy the full equivalent meaning of a code in the source system.
Index of Diseases and Injuries Definitions
- And - The word "and" should be interpreted to mean either "and" or "or" when it appears in a title.
- Code also note - A "code also" note instructs that two codes may be required to fully describe a condition, but this note does not provide sequencing direction.
- Code first - Certain conditions have both an underlying etiology and multiple body system manifestations due to the underlying etiology. For such conditions, the ICD-10-CM has a coding convention that requires the underlying condition be sequenced first followed by the manifestation. Wherever such a combination exists, there is a "use additional code" note at the etiology code, and a "code first" note at the manifestation code. These instructional notes indicate the proper sequencing order of the codes, etiology followed by manifestation.
- Type 1 Excludes Notes - A type 1 Excludes note is a pure excludes note. It means "NOT CODED HERE!" An Excludes1 note indicates that the code excluded should never be used at the same time as the code above the Excludes1 note. An Excludes1 is used when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
- Type 2 Excludes Notes - A type 2 Excludes note represents "Not included here". An excludes2 note indicates that the condition excluded is not part of the condition represented by the code, but a patient may have both conditions at the same time. When an Excludes2 note appears under a code, it is acceptable to use both the code and the excluded code together, when appropriate.
- Includes Notes - This note appears immediately under a three character code title to further define, or give examples of, the content of the category.
- Inclusion terms - List of terms is included under some codes. These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
- NEC "Not elsewhere classifiable" - This abbreviation in the Alphabetic Index represents "other specified". When a specific code is not available for a condition, the Alphabetic Index directs the coder to the "other specified” code in the Tabular List.
- NOS "Not otherwise specified" - This abbreviation is the equivalent of unspecified.
- See - The "see" instruction following a main term in the Alphabetic Index indicates that another term should be referenced. It is necessary to go to the main term referenced with the "see" note to locate the correct code.
- See Also - A "see also" instruction following a main term in the Alphabetic Index instructs that there is another main term that may also be referenced that may provide additional Alphabetic Index entries that may be useful. It is not necessary to follow the "see also" note when the original main term provides the necessary code.
- 7th Characters - Certain ICD-10-CM categories have applicable 7th characters. The applicable 7th character is required for all codes within the category, or as the notes in the Tabular List instruct. The 7th character must always be the 7th character in the data field. If a code that requires a 7th character is not 6 characters, a placeholder X must be used to fill in the empty characters.
- With - The word "with" should be interpreted to mean "associated with" or "due to" when it appears in a code title, the Alphabetic Index, or an instructional note in the Tabular List. The word "with" in the Alphabetic Index is sequenced immediately following the main term, not in alphabetical order.