Disease #03257 (CACD2 (dystrophy, choroidal, areolar, central, type 2 (CACD2)), OMIM:613105)
Official abbreviation |
CACD2 |
Name |
dystrophy, choroidal, areolar, central, type 2 (CACD2) |
OMIM ID |
613105 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
PRPH2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2019-12-17 16:26:44 +01:00 (CET) |
Individuals
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