Enuresis, nocturnal, 2

Preferred Label : Enuresis, nocturnal, 2;

Symbol : ENUR2;

CISMeF acronym : ENUR2;

Type : Phenotype or locus, molecular basis unknown;

Description : For a general description and a discussion of genetic heterogeneity of nocturnal enuresis, see 600631.;

Inheritance : Autosomal dominant (12q13-q21); heterogeneity;

Prefixed ID : %600808;

Details

Origin ID

600808;

UMLS CUI

C1833268;

Currated CISMeF NLP mapping
- enuresis, nocturnal, 2 [MeSH concept]
- enuresis, nocturnal, 2 [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Enuresis nocturna [HPO term]
- Heterogeneous [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- enuresis, nocturnal, 2 [MeSH Supplementary Concept]
- enuresis, nocturnal, 2 [MeSH concept]

Keyword's position in hierarchy(ies) :

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