Other specified congenital malformations of integument

Preferred Label : Other specified congenital malformations of integument;

Inclusion CIM-10 : Aplasia cutis congenita;

Diag associé à un acte (%) : 96.2;

Source : OMS;

Date de début : 01/01/1997;

Details

Origin ID

Q848;

UMLS CUI

C0478090;

Currated CISMeF NLP mapping
- Aplasia Cutis Congenita [NCIt concept]
- Aplasia cutis congenita [ORDO Disease]
- Aplasia cutis congenita [ICD-11 Category]
- Aplasia cutis congenita [HPO term]
- Aplasia cutis congenita [MedDRA Preferred Term]
- Aplasia cutis congenita [PASCAL descriptor]
- Aplasia cutis congenita (disorder) [SNOMED CT concept]
- Aplasia cutis congenita, nonsyndromic [OMIM Phenotype]
- Aplasia of skin (disorder) [SNOMED CT concept]
- Other specified congenital malformations of integument [ICD-10 Sub-category (who)]
- aplasia cutis congenita [MeSH concept]
- aplasia cutis congenita [SNOMED Notion]
- aplasia cutis congenita [Disease (Nov.)]
- ectodermal dysplasia [MeSH Descriptor]
Orphanet concepts
- Aplasia cutis congenita [ORDO Disease]
- Aplasia cutis congenita-intestinal lymphangiectasia syndrome [ORDO Disease]
- Aplasia cutis-myopia syndrome [ORDO Disease]
- Didymosis aplasticosebacea [ORDO Disease]
- NEVADA syndrome [ORDO Disease]
- Odontomicronychial dysplasia [ORDO Disease]
- Recessive aplasia cutis congenita of limbs [ORDO Disease]
- SCALP syndrome [ORDO Disease]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Other specified anomalies of the integument [ICD-9 code]

Keyword's position in hierarchy(ies) :

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