pigment disorder, reticulate

Preferred Label : pigment disorder, reticulate;

Obsolete resource : true;

Approved symbol HGNC : PDR;

Chromosome HGNC : Xp22-p21;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:8817;

UMLS CUI

C1418444;

Automatic exact mappings (from CISMeF team)
- Pigmentary disorder, reticulate, with systemic manifestations, X-linked [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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