OMOP Concept 4301416
Congenital anomaly of digit
StandardConditionSNOMED403855001Disorder
Maps from
1
Descendants
672
Valid from
31 Jul 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital anomaly of digit via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 403855001 | Congenital malformation of digit | Non-standard |
Synonyms
Alternative names recorded for Congenital anomaly of digit across source vocabularies.
- anomalía digital congénita
- anomalía digital congénita (trastorno)
- Congenital anomaly of digit (disorder)
- Congenital malformation of digit
- Developmental anomaly of digits
- malformación congénita de dedo
- Perodactylia
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
Narrower concepts
(672)Included automatically when you query with descendants.
- 1Acrofrontofacionasal dysostosis type 2
- 1Acromelanosis
- 1Acropectorovertebral dysplasia
- 1Adactyly
- 1Autosomal recessive facio-digito-genital syndrome
- 1Bovine hereditary syndactyly
- 1Brachytelephalangy, facial dysmorphism, Kallmann syndrome
- 1Congenital abnormal shape of digit
- 1Congenital anomaly of finger
- 1Congenital anomaly of nail
- 1Congenital anomaly of toe
- 1Congenital macrodactyly
- 1Congenital malformation of thumb
- 1Congenital malposition of digit
- 1Congenital thickening of forepaw phalanx
- 1Congenital thickening of hindpaw phalanx
- 1Ichthyosis, oral and digital anomalies syndrome
- 1Incomplete ossification of forepaw phalanx
- 1Lack of ossification of forepaw phalanx
- 1Microcephalus with albinism and digital anomaly syndrome
- 1Multinodular goiter, cystic kidney, polydactyly syndrome
- 1Neurofaciodigitorenal syndrome
- 1Oculodento-osseous dysplasia
- 1Oculo-palato-digital syndrome
- 1Oral-facial-digital syndrome
- 1Pierre Robin sequence faciodigital anomaly syndrome
- 1Polydactyly
- 1Rudimentary digit
- 1Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome
- 1Symphalangism
- 1Syndactyly
- 1TRAF7-associated heart defect, digital anomalies, facial dysmorphism, motor and speech delay syndrome
- 1Trigonocephaly with bifid nose and acral anomaly syndrome
- 1Trigonocephaly with broad thumb syndrome
- 1Ventricular extrasystoles with syncope, perodactyly and Robin sequence syndrome
- 216p12.1p12.3 triplication syndrome
- 2Absent tibia, polydactyly, arachnoid cyst syndrome
- 2Acrocephalosyndactyly
- 2Acropectoral syndrome
- 2Acrosyndactyly of toe
- 2Adducted thumbs and arthrogryposis syndrome Christian type
- 2Agenesis of epiphysis of phalanx of toe
- 2Aglossia-adactyly syndrome
- 2Anonychia
- 2Aphalangy and syndactyly with microcephaly syndrome
- 2Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome
- 2Aplasia of phalanx of hand
- 2Arachnodactyly
- 2Autosomal dominant preaxial polydactyly, upper back hypertrichosis syndrome
- 2Bifid digit
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