Disease #02940 (CSRD;CSNB2B (cone-rod synaptic disorder, congenital nonprogressive (CSRD, congenital stationary night blindness, type 2B (CSNB-2B))), OMIM:610427)

Official abbreviation CSRD;CSNB2B
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 Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CABP4
Associated tissues -
Disease features autosomal recessive
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)

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