Nail disorder, nonsyndromic congenital, 2

Preferred Label : Nail disorder, nonsyndromic congenital, 2;

Symbol : NDNC2;

CISMeF acronym : NDNC2;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Koilonychia, hereditary; Spoon nails;

Included titles and symbols : Koilonychia with leukonychia;

Description : Koilonychia, or 'spoon nails,' is a relatively uncommon disorder in which the nails are abnormally thin and concave from side to side, with the edges turned up. Single or multiple fingers and/or toes may be involved (summary by Bumpers and Bishop, 1980). Koilonychia is referred to here as nonsyndromic congenital nail disorder-2 (NDNC2). For a list of other nonsyndromic congenital nail disorders and a discussion of genetic heterogeneity, see NDNC1 (161050).;

Inheritance : Autosomal dominant;

Prefixed ID : %149300;

Détails

Origin ID

149300;

UMLS CUI

C0266000;

Automatic exact mappings (from CISMeF team)
- Hereditary koilonychia [ICD-11 More detail]
- Koilonychia [ICD-11 More detail]
- Koilonychia (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Hereditary koilonychia [MeSH concept]
- hereditary koilonychia [MeSH Supplementary Concept]
- nonsyndromic congenital nail disorder 2 [DO Concept]
DO Cross reference
- nonsyndromic congenital nail disorder 2 [DO Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Concave nail [HPO term]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital koilonychia (disorder) [SNOMED CT concept]
- Hereditary koilonychia [MeSH concept]
- congenital koilonychia [SNOMED Notion]
- hereditary koilonychia [MeSH Supplementary Concept]
- nonsyndromic congenital nail disorder 2 [DO Concept]

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