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

Official abbreviation VMD-5
Name dystrophy, macular, vitelliform, type 5 (VMD-5)
OMIM ID 616152
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene IMPG2
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Disease features -
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Individuals

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00371667 178411 - - F ? Germany - - 0 - - VMD-5 (+) Rod-cone dystrophy,(+) Uveitis,(+) Nyctalopia,(+) Vasculitis IMPG2 IMPG2 1 1 Andreas Laner
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