Visceral neuropathy, familial, 3, autosomal dominant

Preferred Label : Visceral neuropathy, familial, 3, autosomal dominant;

Symbol : VSCN3;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Enteric neuropathy, familial; Pseudoobstruction, chronic intestinal, neuropathic;

Prefixed ID : %609629;

Details

Origin ID

609629;

UMLS CUI

C1864996;

Automatic exact mappings (from CISMeF team)
- autosomal dominant familial visceral neuropathy [DO Concept]
- intestinal Pseudo-Obstruction [MeSH concept]
- intestinal pseudo-obstruction [MeSH Descriptor]
Currated CISMeF NLP mapping
- visceral neuropathy, familial, autosomal dominant [MeSH concept]
- visceral neuropathy, familial, autosomal dominant [MeSH Supplementary Concept]
DO Cross reference
- autosomal dominant familial visceral neuropathy [DO Concept]
ORDO concept(s)
- Chronic intestinal pseudoobstruction [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- visceral neuropathy, familial, autosomal dominant [MeSH Supplementary Concept]
- visceral neuropathy, familial, autosomal dominant [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients