Disease #04519 (VMD5 (dystrophy, macular, vitelliform, type 5 (VMD-5)), OMIM:616152)

Official abbreviation VMD5
Name dystrophy, macular, vitelliform, type 5 (VMD-5)
OMIM ID 616152
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 IMPG2
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00371667 178411 - - F ? Germany - - - - - VMD5 (+) Rod-cone dystrophy,(+) Uveitis,(+) Nyctalopia,(+) Vasculitis IMPG2 IMPG2 1 1 Andreas Laner
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