porencephaly cerebellar hypoplasia malformations

Preferred Label : porencephaly cerebellar hypoplasia malformations;

MeSH synonym : porencephaly, cerebellar hypoplasia, and internal malformations;

Details

Origin ID

C536336;

UMLS CUI

C1832472;

CISMeF manual mappings
- Porencephaly-cerebellar hypoplasia-internal malformations syndrome [ORDO Disease]
Currated CISMeF NLP mapping
- Porencephaly, cerebellar hypoplasia, and internal malformations [OMIM Phenotype]
- Porencephaly, cerebellar hypoplasia, internal malformations syndrome (disorder) [SNOMED CT concept]
MeSH term(s) associated for indexing
- Porencephaly [MeSH Descriptor]
- cerebellar diseases [MeSH Descriptor]
- cerebellum [MeSH Descriptor]
Record concept(s)
- Porencephaly cerebellar hypoplasia malformations [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Porencephaly, cerebellar hypoplasia, and internal malformations [OMIM Phenotype]
- Porencephaly-cerebellar hypoplasia-internal malformations syndrome [ORDO Disease]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients