hydrocephalus, X-Linked, with congenital idiopathic intestinal pseudoobstruction

Preferred Label : hydrocephalus, X-Linked, with congenital idiopathic intestinal pseudoobstruction;

MeSH note : mutation in L1CAM;

Origin ID

C564408;

UMLS CUI

C1844006;

Automatic exact mappings (from CISMeF team)
- Hydrocephalus, congenital, X-linked [OMIM Phenotype]
MeSH term(s) associated for indexing
- genetic diseases, X-linked [MeSH Descriptor]
- hydrocephalus [MeSH Descriptor]
- intestinal pseudo-obstruction [MeSH Descriptor]
Record concept(s)
- hydrocephalus, X-Linked, with congenital idiopathic intestinal pseudoobstruction [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]