Disease #05321 (MYP-2 (myopia, autosomal dominant, type 2 (MYP-2)), OMIM:160700)

Official abbreviation MYP-2
Name myopia, autosomal dominant, type 2 (MYP-2)
OMIM ID 160700
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 0 genes -
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Disease features -
Remarks -