Disease #02016 (ACHM3 (achromatopsia, type 3), OMIM:262300)
Official abbreviation |
ACHM3 |
Name |
achromatopsia, type 3 |
OMIM ID |
262300 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
35 |
Phenotype entries for this disease |
34 |
Associated with 1 gene |
CNGB3 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2024-09-30 14:18:16 +02:00 (CEST) |
Individuals
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