Disease #05957 (MCDR1 (dystrophy, macular, type 1, North Carolina type (MCDR1)), OMIM:136550)
| Official abbreviation |
MCDR1 |
| Name |
dystrophy, macular, type 1, North Carolina type (MCDR1) |
| OMIM ID |
136550 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
9 |
| Phenotype entries for this disease |
7 |
| Associated with 0 genes |
- |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-07-27 12:53:42 +02:00 (CEST) |
| Date last edited |
N/A |
Individuals
|