Lissencephaly, familial, with cleft palate and cerebellar hypoplasia

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

Type : Other, mainly phenotypes with suspected mendelian basis;

Prefixed ID : 604382;

Details

Origin ID

604382;

UMLS CUI

C1858419;

Currated CISMeF NLP mapping
- lissencephaly, familial, with cleft palate and cerebellar hypoplasia [MeSH concept]
- lissencephaly, familial, with cleft palate and cerebellar hypoplasia [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- lissencephaly, familial, with cleft palate and cerebellar hypoplasia [MeSH Supplementary Concept]
- lissencephaly, familial, with cleft palate and cerebellar hypoplasia [MeSH concept]

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