cerebellar vermis aplasia with associated features suggesting Smith-Lemli-Opitz syndrome and meckel syndrome

Preferred Label : cerebellar vermis aplasia with associated features suggesting Smith-Lemli-Opitz syndrome and meckel syndrome;

Origin ID

C565867;

UMLS CUI

C1859300;

Automatic exact mappings (from CISMeF team)
- Cerebellar vermis aplasia with associated features suggesting smith-lemli-opitz syndrome and meckel syndrome [OMIM Phenotype]
MeSH term(s) associated for indexing
- cerebellar diseases [MeSH Descriptor]
- cerebellum [MeSH Descriptor]
- encephalocele [MeSH Descriptor]
- meningocele [MeSH Descriptor]
- polycystic kidney diseases [MeSH Descriptor]
- smith-lemli-opitz syndrome [MeSH Descriptor]
Record concept(s)
- cerebellar vermis aplasia with associated features suggesting Smith-Lemli-Opitz syndrome and meckel syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cerebellar vermis aplasia with associated features suggesting smith-lemli-opitz syndrome and meckel syndrome [OMIM Phenotype]