Disease #02940 (CSRD;CSNB-2B (cone-rod synaptic disorder, congenital nonprogressive (CSRD, congenital stationary night blindness, type 2B (CSNB-2B))), OMIM:610427)

Official abbreviation CSRD;CSNB-2B
Name cone-rod synaptic disorder, congenital nonprogressive (CSRD, congenital stationary night blindness, type 2B (CSNB-2B))
OMIM ID 610427
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene CABP4
Associated tissues -
Disease features autosomal recessive
Remarks -