Disease #01980 (CSNBO1 (Oguchi disease 1 (night blindness, stationary, congenitial, Oguchi type 1 (CSNBO-1))), OMIM:258100)

Official abbreviation CSNBO1
Name Oguchi disease 1 (night blindness, stationary, congenitial, Oguchi type 1 (CSNBO-1))
OMIM ID 258100
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene SAG
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00095929 61029 PubMed: Li 2017 - M yes Pakistan Pakistani - - - - CSNBO1 - GRK1 GRK1 1 1 James Hejtmancik
00411363 195271 - - M - Germany - - - - - CSNBO1 Myopia, High myopia, Unilateral cryptorchidism, Hemangioma NYX NYX 1 1 Andreas Laner
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