Disease #02225
Official abbreviation |
CBBM;COD-5 |
Name |
monochromacy, blue cone (CBBM, cone dystrophy, type 5 (COD-5)) |
OMIM ID |
303700 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
0 |
Phenotype entries for this disease |
0 |
Associated with 2 genes |
OPN1LW, OPN1MW |
Associated tissues |
- |
Disease features |
X-linked recessive |
Remarks |
- |
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