OMOP Concept 134741
Congenital anomaly of limb
StandardConditionSNOMED60475009Disorder
Maps from
34
Descendants
1,696
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
34 source codes normalize to Congenital anomaly of limb via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Congenital anomaly of limb across source vocabularies.
- anomalía congénita de una extremidad
- anomalía congénita de una extremidad (trastorno)
- Congenital abnormality of the limb
- Congenital anomaly of limb (disorder)
- Congenital deformity of limb
- deformidad congénita de un miembro
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(8)Roll up to these when you need a wider cohort.
Narrower concepts
(1,696)Included automatically when you query with descendants.
- 114q22q23 microdeletion syndrome
- 15-amino-4-imidazole carboxamide ribosiduria
- 1Acrorenal syndrome
- 1Adams-Oliver syndrome
- 1Agenesis of both forepaws and both hindpaws
- 1Anisomelia
- 1Aplasia of limb
- 1Campomelia Cumming type
- 1Carpotarsal osteochondromatosis
- 1CHILD syndrome
- 1Congenital anomaly of blood vessel of limb
- 1Congenital anomaly of digit
- 1Congenital anomaly of lower limb
- 1Congenital anomaly of paw
- 1Congenital anomaly of upper limb
- 1Congenital dysplasia of limb
- 1Congenital hyperextension of limb
- 1Congenital hyperflexion of limb
- 1Congenital malrotation of limb
- 1Congenital primary lymphedema of Gordon
- 1Congenital pseudoarthrosis of limb
- 1Constricting band of extremity
- 1Fuhrmann syndrome
- 1Grebe syndrome
- 1Hennekam syndrome
- 1Longitudinal deficiency of limb
- 1Longitudinal deficiency of part of limb
- 1Lymphedema hypoparathyroidism syndrome
- 1Macromelia
- 1Micromelia
- 1Mullerian duct and limb anomalies syndrome
- 1Multiple malformation syndrome with facial-limb defects as major feature
- 1Myofibrillar hypoplasia
- 1Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome
- 1Oto-palato-digital syndrome, type I
- 1Oto-palato-digital syndrome, type II
- 1Partial congenital absence of limb
- 1PHAVER syndrome
- 1Polymelia
- 1Symmetrical dyschromatosis of extremities
- 1Waardenburg syndrome type 3
- 216p12.1p12.3 triplication syndrome
- 220q11.2 microdeletion syndrome
- 24q25 proximal deletion syndrome
- 2Aase Smith type 1 syndrome
- 2Aberrant muscle of the lower limb
- 2Aberrant muscle of the upper limb
- 2Absence deformity of leg and congenital cataract syndrome
- 2Absent radius, anogenital anomalies syndrome
- 2Accessory carpal bones
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