cerebellar atrophy with progressive microcephaly

Preferred Label : cerebellar atrophy with progressive microcephaly;

Obsolete resource : true;

Approved symbol HGNC : CLAM;

Alias symbols HGNC : PCH3;

Chromosome HGNC : 7q11-q21;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:20394;

UMLS CUI

C1538471;

Automatic exact mappings (from CISMeF team)
- Pontocerebellar hypoplasia, type 3 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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