Disease #00363 (MYPBB (myopathy, congenital, Baily-Bloch), OMIM:255995)

Official abbreviation MYPBB
Name myopathy, congenital, Baily-Bloch
OMIM ID 255995
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene STAC3
Associated tissues -
Disease features -
Remarks -
Date created 2014-03-27 19:33:47 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00016373 - PubMed: Horstick 2013 5 families, 13 affecteds, unaffected carrier parents ? ? United States native American - - - - MYPBB see paper STAC3 STAC3 1 15 Johan den Dunnen
00081032 - PubMed: Trujillano 2017 no information from parents - - - - - - - - MYPBB Native American myopathy (OMIM:255995) STAC3 STAC3 1 1 Daniel Trujillano
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