Disease #02016 (ACHM-3 (achromatopsia, type 3 (ACHM-3)), OMIM:262300)

Official abbreviation ACHM-3
Name achromatopsia, type 3 (ACHM-3)
OMIM ID 262300
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CNGB3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited N/A