Disease #00023 (DM (Myotonic Dystrophy), OMIM:160900)

Official abbreviation DM
Name Myotonic Dystrophy
OMIM ID 160900
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -

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