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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