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Standards Ontologies Notations
partial central choroid dystrophy

Summary
Synonym
  • Choroidal dystrophy, central areolar
Super Class
hereditary choroidal atrophy
Disease Ontology
DOID:9822
Mondo Disease Ontology
UMLS
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5961 PRPH2 peripherin 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
19133 Prph2 peripherin 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
25534 Prph2 peripherin 2
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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024