Anomaly, anomalous (congenital) (unspecified type) Q89.9 Alder (-Reilly) (leukocyte granulation)
D72.0 coarctation (preductal) (postductal)
Q25.1 aortic cusp or valve
Q23.9 apple peel syndrome
Q41.1 aqueduct of Sylvius
Q03.0 with spina bifida see Spina bifida, with hydrocephalus
arteriovenous NEC
acquired see Angiodysplasia
artery (peripheral)
Q27.9 aryteno-epiglottic folds
Q31.8 atrial
atrioventricular
auricle
causing impairment of hearing
Q16.9 band
biliary duct or passage
Q44.5 with
encephalocele see Encephalocele
with spina bifida see Spina bifida, by site, with hydrocephalus
cardiovascular system
Q28.8 Chédiak-Higashi (-Steinbrinck) (congenital gigantism of peroxidase granules)
E70.330 chromosomes, chromosomal
Q99.9 D (1) see condition, chromosome 13
E (3) see condition, chromosome 18
G see condition, chromosome 21
sex
gonadal dysgenesis (pure)
Q99.1 specified NEC
Q99.8 Non-billable communication
left ventricle with right atrium
Q21.0 connection
renal artery with kidney
Q27.2 coronary artery or vein
Q24.5 cranium see Anomaly, skull
dental
alveolar see Anomaly, alveolar
alveolar see Anomaly, alveolar
dental arch relationship
M26.20 jaw-cranial base relationship
M26.10 mandibular
maxillary
dental arch relationship NEC
M26.29 jaw-cranial base relationship see Anomaly, dentofacial, jaw-cranial base relationship
jaw size see Anomaly, dentofacial, jaw size
temporomandibular joint
M26.60- Non-billable articular disc
M26.63- Non-billable tooth position, fully erupted
M26.30 diaphragm (apertures) NEC
Q79.1 digestive organ (s) or tract
Q45.9 distance, interarch (excessive) (inadequate)
M26.25 distribution, coronary artery
Q24.5 ductus
causing impairment of hearing
Q16.9 middle (causing impairment of hearing)
Q16.4 Ebstein's (heart) (tricuspid valve)
Q22.5 Eisenmenger's (ventricular septal defect)
Q21.8 endocrine gland NEC
Q89.2 fixation, intestine
Q43.3 flexion (joint) NOS
Q74.9 varus (congenital)
Q66.3- Non-billable foramen
frontal bone see Anomaly, skull
gallbladder (position) (shape) (size)
Q44.1 gastrointestinal tract
Q45.9 genitalia, genital organ (s) or system
genitourinary NEC
granulation or granulocyte, genetic (constitutional) (leukocyte)
D72.0 head see Anomaly, skull
fibroelastosis cordis
I42.4 patent ductus arteriosus (Botalli)
Q25.0 with pulmonary stenosis or atresia, dextraposition of aorta and hypertrophy of right ventricle
Q21.3 with pulmonary stenosis or atresia, dextraposition of aorta and hypertrophy of right ventricle
Q21.3 tetralogy of Fallot
Q21.3 aortic
functional, with stenosis see Stenosis, aortic (valve)
mitral
tricuspid
hydatid of Morgagni
hypersegmentation of neutrophils, hereditary
D72.0 ileocecal (coil) (valve)
Q43.9 interarch distance (excessive) (inadequate)
M26.25 intervertebral cartilage or disc
Q76.49 intestine (large) (small)
Q43.9 with anomalous adhesions, fixation or malrotation
Q43.3 jaw see Anomaly, dentofacial
alveolar see Anomaly, alveolar
jaw-cranial base relationship see Anomaly, dentofacial, jaw-cranial base relationship
kidney (s) (calyx) (pelvis)
Q63.9 Klippel-Feil (brevicollis)
Q76.1 labyrinth, membranous
Q16.5 lacrimal apparatus or duct
Q10.6 larynx, laryngeal (muscle)
Q31.9 leukocytes, genetic
D72.0 granulation (constitutional)
D72.0 reduction deformity see Defect, reduction, lower limb
lumbosacral (joint) (region)
Q76.49 kyphosis see Kyphosis, congenital
lordosis see Lordosis, congenital
lung (fissure) (lobe)
Q33.9 mandible see Anomaly, dentofacial
maxilla see Anomaly, dentofacial
meningeal bands or folds
Q07.9 mitral (leaflets) (valve)
Q23.9 Müllerian see also Anomaly, by site
musculoskeletal system, except limbs
Q79.9 nervous system (central)
Q07.9 nose, nasal (bones) (cartilage) (septum) (sinus)
Q30.9 omphalomesenteric duct
Q43.0 opening, pulmonary veins
Q26.4 optic
opticociliary vessels
Q13.2 origin
artery
osseous meatus (ear)
Q16.1 palate (hard) (soft) NEC
Q38.5 pancreas or pancreatic duct
Q45.3 Pelger-Huët (hereditary hyposegmentation)
D72.0 peripheral vascular system
Q27.9 position, tooth, teeth, fully erupted
M26.30 reduction (extremity) (limb)
femur (longitudinal) see Defect, reduction, lower limb, longitudinal, femur
fibula (longitudinal) see Defect, reduction, lower limb, longitudinal, fibula
lower limb see Defect, reduction, lower limb
radius (longitudinal) see Defect, reduction, upper limb, longitudinal, radius
tibia (longitudinal) see Defect, reduction, lower limb, longitudinal, tibia
ulna (longitudinal) see Defect, reduction, upper limb, longitudinal, ulna
upper limb see Defect, reduction, upper limb
refraction see Disorder, refraction
rotation see Malrotation
sacroiliac (joint) NEC
Q74.2 kyphosis see Kyphosis, congenital
lordosis see Lordosis, congenital
saddle nose, syphilitic
A50.57 salivary duct or gland
Q38.4 scrotum see Malformation, testis and scrotum
sex chromosomes NEC see also Anomaly, chromosomes
shoulder (girdle) (joint)
Q74.0 skeleton generalized
Q78.9 with
encephalocele see Encephalocele
with spina bifida see Spina bifida, by site, with hydrocephalus
specified organ or site NEC
Q89.89 kyphosis see Kyphosis, congenital
lordosis see Lordosis, congenital
testis see Malformation, testis and scrotum
position, fully erupted
M26.30 trachea (cartilage)
Q32.1 tricuspid (leaflet) (valve)
Q22.9 atresia or stenosis
Q22.4 Uhl's (hypoplasia of myocardium, right ventricle)
Q24.8 union
cricoid cartilage and thyroid cartilage
Q31.8 thyroid cartilage and hyoid bone
Q31.8 trachea with larynx
Q31.8 with only one functioning horn
Q51.4 venae cavae inferioris
Q24.8 vein (s) (peripheral)
Q27.9 vena cava (inferior) (superior)
Q26.9 venous see Anomaly, vein(s)
ventricular
kyphosis see Kyphosis, congenital
lordosis see Lordosis, congenital
vitreous body or humor
Q14.0