Disease #01455

Official abbreviation MPD-1
Name myopathy, distal, type 1 (MPD-1)
OMIM ID 160500
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene MYH7
Associated tissues -
Disease features -
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Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00056376 - PubMed: Melberg 2010 affected mother and daugther F - - Sweden - 0 - - MPD-1 centronuclear myopathy, neonatal-onset DNM2 DNM2 1 2 Johan den Dunnen
00056377 - - - - - - - - 0 - - MPD-1 centronuclear myopathy with cataracts DNM2 DNM2 1 1 Johan den Dunnen
00306205 103 - - M - China - - - - - MPD-1 - MYH7 MYH7 1 1 Sha Hong
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