Disease #01456 (TAM1 (myopathy, tubular aggregates, type 1 (TAM-1)), OMIM:160565)

Official abbreviation TAM1
Name myopathy, tubular aggregates, type 1 (TAM-1)
OMIM ID 160565
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 11
Phenotype entries for this disease 8
Associated with 1 gene STIM1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

11 entries on 1 page. Showing entries 1 - 11.
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00106535 - - 3-generation family - no Germany - - - - - TAM1 - - CASQ1 1 1 Johann Böhm
00106536 103901 - - M no - - - - - - TAM1 - - CASQ1 1 1 Johann Böhm
00234377 - - - M no France - - - - - TAM1 - STIM1 STIM1 1 1 Johann Böhm
00234378 - - - F ? Italy - - - - - TAM1 - STIM1 STIM1 1 1 Johann Böhm
00234379 - - - F yes Eritrea - - - - - TAM1 - STIM1 STIM1 1 1 Johann Böhm
00266381 1.II.2 PubMed: Morin 2019 - M no France - - - - - TAM1 Axial muscle weakness, myalgia, diabetes, hypertension, lipodystrophy, coronary artery disease. Muscle biopsy: tubular aggregates, fiber size variability, type I fiber predominance, internal nuclei STIM1 STIM1 1 1 Johann Böhm
00266385 - PubMed: Bohm 2014 - M yes Italy - - - - - TAM1 Lower limb weakness, myalgia, eye movement defects. Muscle biopsy: tubular aggregates, fiber size variability, internal nuclei, fibrosis - STIM1 1 1 Johann Böhm
00269322 I.1 PubMed: Walter 2015 - M no Germany - - - - - TAM1 - STIM1 STIM1 1 1 Johann Böhm
00271177 Fam1PatII1 PubMed: Böhm 2013 - M no - - - - - - TAM1 Upper and lower limb muscle weakness, eye movement defects, contractures - STIM1 1 1 Johann Böhm
00271178 - PubMed: Noury 2017 - F no Portugal - - - - - TAM1 Lower limb muscle weakness, cramps, eye movement defects, contractures, asplenia, short stature, hypocalcemia, anemia, tooth enamel hypocalcification, - STIM1 1 1 Johann Böhm
00466395 - Pending - F - France - - - - - TAM1 Limb-girdle muscular dystrophy * Motor delay * Hyperlordosis * Muscle fiber necrosis * Increased endomysial connective tissue * Abnormal circulating creatine kinase concentration * Specific learning disability - STIM1 1 1 Camille Verebi
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