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;

Détails

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]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients