Disease #00109 (WDM (myopathy, distal, Welander (WDM)), OMIM:604454)

Official abbreviation WDM
Name myopathy, distal, Welander (WDM)
OMIM ID 604454
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant, Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene TIA1
Associated tissues -
Disease features -
Remarks -
Date created 2013-01-29 13:42:56 +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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00000354 - - - - - - - - - - - WDM - - TIA1 1 46 Joakim Klar
00006906 - - - - ? Netherlands - - - - - ACG1B, AO2, cancer, breast, cancer, predisposition, DYT, EDM4, EHT, MRLIAF, NBIA4, TMAU, TMD, WDM - BRCA1, BRCA2 BRCA1 1 1 Marjolijn JL Ligtenberg
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