Disease #06171 (CSNB1H (Night blindness, congenital stationary, type 1H), OMIM:617024)

Official abbreviation CSNB1H
Name Night blindness, congenital stationary, type 1H
OMIM ID 617024
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene GNB3
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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