Cerebelloparenchymal disorder II

Preferred Label : Cerebelloparenchymal disorder II;

Obsolete resource : true;

Moved to : 607136;

Symbol : CPD2;

CISMeF acronym : CPD2;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Cpd, late-onset recessive type;

Inheritance : Autosomal recessive;

Prefixed ID : 213100;

Details

Origin ID

213100;

UMLS CUI

C1859299;

Automatic exact mappings (from CISMeF team)
- spinocerebellar ataxias [MeSH Descriptor]
Currated CISMeF NLP mapping
- cerebelloparenchymal disorder II [MeSH concept]
- cerebelloparenchymal disorder II [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- cerebelloparenchymal disorder II [MeSH Supplementary Concept]
- cerebelloparenchymal disorder II [MeSH concept]

Keyword's position in hierarchy(ies) :

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