Disease #02332 (CORD5 (dystrophy, cone-rod, type 5 (CORD5)), OMIM:600977)
Official abbreviation |
CORD5 |
Name |
dystrophy, cone-rod, type 5 (CORD5) |
OMIM ID |
600977 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
35 |
Phenotype entries for this disease |
35 |
Associated with 1 gene |
PITPNM3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2020-11-03 17:11:25 +01:00 (CET) |
Individuals
|