Disease #01601 (SVD (vitreoretinal degeneration, snwoflake type (SVD)), OMIM:193230)

Official abbreviation SVD
Name vitreoretinal degeneration, snwoflake type (SVD)
OMIM ID 193230
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene KCNJ13
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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00034370 - PubMed: Hejtmancik 2008 multi-generation family, 13 affecteds - - United States European, white - - - - SVD see paper; affecteds 12-85y, fibrillar degeneration vitreous humor, early-onset cataract, minute crystalline deposits neurosensory retina, retinal detachment KCNJ13 KCNJ13 1 13 Johan den Dunnen
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