Disease #01471

Official abbreviation CSNBAD-2
Name blindness, night, stationary, congenital, autosomal dominant, type 2 (CSNBAD-2)
OMIM ID 163500
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene PDE6B
Associated tissues -
Disease features -
Remarks -