lissencephaly, familial, with cleft palate and cerebellar hypoplasia

Preferred Label : lissencephaly, familial, with cleft palate and cerebellar hypoplasia;

Origin ID

C565781;

UMLS CUI

C1858419;

Currated CISMeF NLP mapping
- Lissencephaly, familial, with cleft palate and cerebellar hypoplasia [OMIM Phenotype]
MeSH term(s) associated for indexing
- cerebellum [MeSH Descriptor]
- cleft palate [MeSH Descriptor]
- lissencephaly [MeSH Descriptor]
Record concept(s)
- lissencephaly, familial, with cleft palate and cerebellar hypoplasia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Lissencephaly, familial, with cleft palate and cerebellar hypoplasia [OMIM Phenotype]