Disease #03059 (VMD2 (dystrophy, macular, vitelliform, type 2 (VMD-2 (Best macular dystrophy (BMD))), OMIM:153700)

Official abbreviation VMD2
Name dystrophy, macular, vitelliform, type 2 (VMD-2 (Best macular dystrophy (BMD))
OMIM ID 153700
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene BEST1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-04-30 09:01:13 +02:00 (CEST)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00155391 - Sharon, submitted - M yes Israel Arab-Muslim - - - - VMD2 - BEST1 BEST1 1 2 Dror Sharon
00155392 - Sharon, submitted - F no Israel Jewish-Ashkenazi - - - - VMD2 - BEST1 BEST1 1 2 Dror Sharon
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