Disease #04468 (EOMD (macular degeneration, early-onset (EOMD)), OMIM:616118)

Official abbreviation EOMD
Name macular degeneration, early-onset (EOMD)
OMIM ID 616118
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene FBN2
Associated tissues -
Disease features -
Remarks -