ICD-9 Diagnosis Code 759.89

Specfied cong anomal NEC

Diagnosis Code 759.89

ICD-9: 759.89
Short Description: Specfied cong anomal NEC
Long Description: Other specified congenital anomalies
This is the 2014 version of the ICD-9-CM diagnosis code 759.89

Code Classification
  • Congenital anomalies (740–759)
    • Congenital anomalies (740-759)
      • 759 Other and unspecified congenital anomalies

Information for Medical Professionals

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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 of Diseases and Injuries
References found for the code 759.89 in the Index of Diseases and Injuries:


Information for Patients


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. To find others, like heart defects, doctors use special tests. Birth defects can vary from mild to severe. Some result from exposures to medicines or chemicals. For example, alcohol abuse can cause fetal alcohol syndrome. Infections during pregnancy can also result in birth defects. For most birth defects, the cause is unknown.

Some birth defects can be prevented. Taking folic acid can help prevent some birth defects. Talk to your doctor about any medicines you take. Some medicines can cause serious birth defects.

Babies with birth defects may need surgery or other medical treatments. Today, doctors can diagnose many birth defects in the womb. This enables them to treat or even correct some problems before the baby is born.

Centers for Disease Control and Prevention

  • Intersex


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