cerebellar hypoplasia

Preferred Label : cerebellar hypoplasia;

Details

Origin ID

C562568;

UMLS CUI

C0266470;

Automatic exact mappings (from CISMeF team)
- cerebellar hypoplasia [DO Concept]
Currated CISMeF NLP mapping
- Cerebellar hypoplasia [HPO term]
- Cerebellar hypoplasia [MedDRA Preferred Term]
- Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay [OMIM Phenotype]
- Congenital cerebellar hypoplasia (disorder) [SNOMED CT concept]
- HYPOPLASIA CEREBELLAR [WHO-ART Preferred Term]
- Hypoplasia cerebellar [MedDRA LLT]
- Isolated cerebellar agenesis [ORDO Disease]
- congenital cerebellar hypoplasia [SNOMED Notion]
DO Cross reference
- cerebellar hypoplasia [DO Concept]
HPO term
- Cerebellar hypoplasia [HPO term]
MeSH term(s) associated for indexing
- cerebellum [MeSH Descriptor]
- developmental disabilities [MeSH Descriptor]
- nervous system malformations [MeSH Descriptor]
Record concept(s)
- cerebellar hypoplasia [MeSH concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Cerebellar hypoplasia [MedDRA Preferred Term]
- Cerebellar hypoplasia [HPO term]
- Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay [OMIM Phenotype]
- Congenital Cerebellar Hypoplasia [NCIt concept]
- Congenital cerebellar hypoplasia (disorder) [SNOMED CT concept]
- HYPOPLASIA CEREBELLAR [WHO-ART Preferred Term]
- Hypoplasia cerebellar [MedDRA LLT]
- Isolated cerebellar agenesis [ORDO Disease]
- congenital cerebellar hypoplasia [SNOMED Notion]
Validated automatic mappings to BTNT
- Congenital Cerebellar Hypoplasia [NCIt concept]

Keyword's position in hierarchy(ies) :

Main resources

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