Disease #04518 (VMD4 (dystrophy, macular, vitelliform, type 4 (VMD-4)), OMIM:616151)

Official abbreviation VMD4
Name dystrophy, macular, vitelliform, type 4 (VMD-4)
OMIM ID 616151
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene IMPG1
Associated tissues -
Disease features -
Remarks -

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