hypoparathyroidism

Preferred Label : hypoparathyroidism;

Obsolete resource : true;

Approved symbol HGNC : HPT;

Alias symbols HGNC : HYPX;

Chromosome HGNC : Xq27;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:5165;

UMLS CUI

C1384672;

Automatic exact mappings (from CISMeF team)
- Hypoparathyroidism, X-linked [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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