Nail disorder, nonsyndromic congenital, 5

Preferred Label : Nail disorder, nonsyndromic congenital, 5;

Symbol : NDNC5;

CISMeF acronym : NDNC5;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Onycholysis, hereditary distal; Onycholysis, partial, with scleronychia;

Description : Hereditary distal onycholysis is an autosomal dominant nail disorder characterized by a decreased rate of growth of the nail, scleronychia, and a straight or concave proximal edge of detachment. Clinical features may include palmoplantar hyperhydrosis and marked sensitivity of the fingers to cold (summary by Bazex et al., 1990). Hereditary distal onycholysis is referred to here as nonsyndromic congenital nail disorder-5 (NDNC5). For a list of other nonsyndromic congenital nail disorders and a discussion of genetic heterogeneity, see NDNC1 (161050).;

Inheritance : Autosomal dominant;

Prefixed ID : %164800;

Details

Origin ID

164800;

UMLS CUI

C1833909;

Automatic exact mappings (from CISMeF team)
- Hereditary distal onycholysis [ICD-11 More detail]
Currated CISMeF NLP mapping
- Hereditary distal onycholysis (disorder) [SNOMED CT concept]
- nonsyndromic congenital nail disorder 5 [DO Concept]
- onycholysis, partial, with scleronychia [MeSH concept]
- onycholysis, partial, with scleronychia [MeSH Supplementary Concept]
DO Cross reference
- nonsyndromic congenital nail disorder 5 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Onycholysis of distal fingernails [HPO term]
- Palmoplantar hyperhidrosis [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary distal onycholysis (disorder) [SNOMED CT concept]
- nonsyndromic congenital nail disorder 5 [DO Concept]
- onycholysis, partial, with scleronychia [MeSH Supplementary Concept]
- onycholysis, partial, with scleronychia [MeSH concept]

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