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
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