glaucoma-related pigment dispersion syndrome 1

Preferred Label : glaucoma-related pigment dispersion syndrome 1;

Obsolete resource : true;

Approved symbol HGNC : GPDS1;

Chromosome HGNC : 7q35-q36;

Locus type HGNC : phenotype;

Détails

Origin ID

HGNC:4457;

UMLS CUI

C1415201;

Automatic exact mappings (from CISMeF team)
- Ocular pigment dispersion with or without glaucoma [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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