Disease #01976 (CSNB1B (blindness, night, stationary, congenital, type 1B (CSNB-1B)), OMIM:257270)

Official abbreviation CSNB1B
Name blindness, night, stationary, congenital, type 1B (CSNB-1B)
OMIM ID 257270
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene GRM6
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

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00059923 - - 1 familie M yes India Indian - - - - CSNB1B - GRM6 GRM6 1 1 Soumittra Nagasamy
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