Disease #02140 (CSNB2A (blindness, night, stationary, congenital, type 2A (CSNB-2A)), OMIM:300071)

Official abbreviation CSNB2A
Name blindness, night, stationary, congenital, type 2A (CSNB-2A)
OMIM ID 300071
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene CACNA1F
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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00382138 269 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - CSNB2A retinal dystrophy; MIM, 300071, 300600, or 300476 CACNA1F CACNA1F 1 1 LOVD
00382140 274 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - CSNB2A retinal dystrophy; MIM, 300071, 300600, or 300476 CACNA1F CACNA1F 1 1 LOVD
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