Alphabetic Index · main term
Anomaly, anomalous (congenital) (unspecified type)
At the main termQ89.9
Anomaly, anomalous (congenital) (unspecified type) is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists Q89.9 for the term on its own. It has 631 subterms and 560 code entries. First-level subterms include abdominal wall NEC, acoustic nerve, adrenal, Alder, alimentary tract, alveolar, ankle, anus and more. Confirm any code you find here in the Tabular List before you report it.
Subterms 631
- abdominal wall NECQ79.59
- acoustic nerveQ07.8
- adrenal (gland)Q89.1
- Alder (-Reilly) (leukocyte granulation)D72.0
- ankle (joint)Q74.2
- anusQ43.9
- aortic cusp or valveQ23.9
- appendixQ43.8
- apple peel syndromeQ41.1
aqueduct of SylviusQ03.0
- with spina bifida see Spina bifida, with hydrocephalus
- armQ74.0
arteriovenous NEC
- coronaryQ24.5
gastrointestinalQ27.33
- acquired see Angiodysplasia
artery (peripheral)Q27.9
- aryteno-epiglottic foldsQ31.8
- auditory canalQ17.8
- Axenfeld'sQ15.0
- backQ89.9
- Bartholin's ductQ38.4
- biliary duct or passageQ44.5
- breastQ83.9
- broad ligamentQ50.6
- bronchusQ32.4
- bulbus cordisQ21.9
- bursaQ79.9
- canal of NuckQ52.4
- canthusQ10.3
- capillaryQ27.9
- cardiovascular systemQ28.8
- carpusQ74.0
- caruncle, lacrimalQ10.6
- cascade stomachQ40.2
- cauda equinaQ06.3
- cecumQ43.9
- cervixQ51.9
- Chédiak-Higashi (-Steinbrinck) (congenital gigantism of peroxidase granules)E70.330
- cheekQ18.9
- chinQ18.9
- chordae tendineaeQ24.8
chromosomes, chromosomalQ99.9
- D (1) see condition, chromosome 13
- E (3) see condition, chromosome 18
- G see condition, chromosome 21
- specified NECQ99.8
- ciliaQ10.3
- circulatory systemQ28.9
- clavicleQ74.0
- clitorisQ52.6
- coccyxQ76.49
- colonQ43.9
- common ductQ44.5
- concha (ear)Q17.3
- cornea (shape)Q13.4
- coronary artery or veinQ24.5
- cranium see Anomaly, skull
- cricoid cartilageQ31.8
- cystic ductQ44.5
dental
- alveolar see Anomaly, alveolar
dentofacialM26.9
- alveolar see Anomaly, alveolar
malocclusionM26.4
- dental arch relationship NECM26.29
- jaw-cranial base relationship see Anomaly, dentofacial, jaw-cranial base relationship
- jaw size see Anomaly, dentofacial, jaw size
- specified type NECM26.89
- dermatoglyphicQ82.8
- diaphragm (apertures) NECQ79.1
- distance, interarch (excessive) (inadequate)M26.25
- distribution, coronary arteryQ24.5
- duodenumQ43.9
- Ebstein's (heart) (tricuspid valve)Q22.5
- ectodermalQ82.9
- Eisenmenger's (ventricular septal defect)Q21.8
- ejaculatory ductQ55.4
- elbowQ74.0
- endocrine gland NECQ89.2
- epididymisQ55.4
- epiglottisQ31.8
- esophagusQ39.9
- eustachian tubeQ17.8
- eyebrowQ18.8
- fallopian tubeQ50.6
- fasciaQ79.9
- femur NECQ74.2
- fibula NECQ74.2
- fingerQ74.0
- fixation, intestineQ43.3
- forearmQ74.0
- foreheadQ75.8
- form, teethK00.2
- fovea centralisQ14.1
- frontal bone see Anomaly, skull
- gallbladder (position) (shape) (size)Q44.1
- Gartner's ductQ52.4
- gastrointestinal tractQ45.9
- GerbodeQ21.0
- glottisQ31.8
- granulation or granulocyte, genetic (constitutional) (leukocyte)D72.0
- gumQ38.6
- gyriQ07.9
- hairQ84.2
- handQ74.0
- hard tissue formation in pulpK04.3
- head see Anomaly, skull
heartQ24.9
- heel NECQ74.2
- Hegglin'sD72.0
- hemianencephalyQ00.0
- hemicephalyQ00.0
- hemicraniaQ00.0
- hepatic ductQ44.5
- hip NECQ74.2
- hourglass stomachQ40.2
- humerusQ74.0
- hymenQ52.4
- hypersegmentation of neutrophils, hereditaryD72.0
- hypophysealQ89.2
- ileocecal (coil) (valve)Q43.9
- ileumQ43.9
- ilium NECQ74.2
- interarch distance (excessive) (inadequate)M26.25
- intervertebral cartilage or discQ76.49
- irisQ13.2
- ischium NECQ74.2
jaw see Anomaly, dentofacial
- alveolar see Anomaly, alveolar
- jaw-cranial base relationship see Anomaly, dentofacial, jaw-cranial base relationship
- jejunumQ43.8
- Jordan'sD72.0
- Klippel-Feil (brevicollis)Q76.1
- kneeQ74.1
- labium (majus) (minus)Q52.70
- labyrinth, membranousQ16.5
- lacrimal apparatus or ductQ10.6
- lensQ12.9
- lid (fold)Q10.3
limbQ74.9
lower NECQ74.2
- reduction deformity see Defect, reduction, lower limb
- upperQ74.0
- lipQ38.0
- lower limb NECQ74.2
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
- May (-Hegglin)D72.0
- meatus urinarius NECQ64.79
- meningoceleQ05.9
- mesenteryQ45.9
- metacarpusQ74.0
- metatarsus NECQ74.2
- mouthQ38.6
Müllerian see also Anomaly, by site
- uterus NECQ51.818
- multiple NECQ89.7
- musculoskeletal system, except limbsQ79.9
- myocardiumQ24.8
- nailQ84.6
- narrowness, eyelidQ10.3
- nasal sinus (wall)Q30.8
- neck (any part)Q18.9
- nervous system (central)Q07.9
- nippleQ83.9
- ocular muscleQ15.8
- omphalomesenteric ductQ43.0
- opening, pulmonary veinsQ26.4
- opticociliary vesselsQ13.2
- orbit (eye)Q10.7
- osseous meatus (ear)Q16.1
- ovaryQ50.39
- oviductQ50.6
- palate (hard) (soft) NECQ38.5
- pancreas or pancreatic ductQ45.3
- papillary musclesQ24.8
- parathyroid glandQ89.2
- paraurethral ductsQ64.79
- parotid (gland)Q38.4
- patellaQ74.1
- Pelger-Huët (hereditary hyposegmentation)D72.0
- pelvic girdle NECQ74.2
- penis (glans)Q55.69
- pericardiumQ24.8
- peripheral vascular systemQ27.9
- Peter'sQ13.4
- pharynxQ38.8
- pituitary (gland)Q89.2
- pleural (folds)Q34.0
- precerebral vesselQ28.1
- prepuceQ55.69
- prostateQ55.4
- pylorusQ40.3
- radiusQ74.0
- rectumQ43.9
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
- retinaQ14.1
- RiegerQ13.81
rotation see Malrotation
- hip or thighQ65.89
- round ligamentQ52.8
- sacroiliac (joint) NECQ74.2
sacrum NECQ76.49
- kyphosis see Kyphosis, congenital
- lordosis see Lordosis, congenital
- saddle nose, syphiliticA50.57
- salivary duct or glandQ38.4
- scapulaQ74.0
- scrotum see Malformation, testis and scrotum
- sebaceous glandQ82.9
- seminal vesiclesQ55.4
- sense organs NECQ07.8
sex chromosomes NEC see also Anomaly, chromosomes
- shoulder (girdle) (joint)Q74.0
- sigmoid (flexure)Q43.9
- simian creaseQ82.8
- sinus of ValsalvaQ25.49
- skeleton generalizedQ78.9
- skin (appendage)Q82.9
skullQ75.9
with
- anencephalyQ00.0
- encephalocele see Encephalocele
hydrocephalusQ03.9
- with spina bifida see Spina bifida, by site, with hydrocephalus
- microcephalyQ02
- specified organ or site NECQ89.89
- spermatic cordQ55.4
spine, spinal NECQ76.49
column NECQ76.49
- kyphosis see Kyphosis, congenital
- lordosis see Lordosis, congenital
- cordQ06.9
- nerve rootQ07.8
- stenonian ductQ38.4
- sternum NECQ76.7
- stomachQ40.3
- submaxillary glandQ38.4
- tarsus NECQ74.2
- tendonQ79.9
- testis see Malformation, testis and scrotum
- thigh NECQ74.2
- throatQ38.8
- thumbQ74.0
- thymus glandQ89.2
- toeQ74.2
- tongueQ38.3
- trachea (cartilage)Q32.1
- tragusQ17.9
- Uhl's (hypoplasia of myocardium, right ventricle)Q24.8
- ulnaQ74.0
- umbilical arteryQ27.0
- upper limbQ74.0
- urachusQ64.4
- urinary tractQ64.9
- uvulaQ38.5
- vaginaQ52.4
- valleculaeQ31.8
- vas deferensQ55.4
- vena cava (inferior) (superior)Q26.9
- venous see Anomaly, vein(s)
- venous returnQ26.8
vertebraQ76.49
- kyphosis see Kyphosis, congenital
- lordosis see Lordosis, congenital
- vesicourethral orificeQ64.79
- vitelline ductQ43.0
- vitreous body or humorQ14.0
- vulvaQ52.70
- wrist (joint)Q74.0