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

8 entries on 1 page. Showing entries 1 - 8.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000087159 - - - Familial, autosomal dominant - - - - - Johann Böhm 00106535
0000087160 - - - Isolated (sporadic) - - - - - Johann Böhm 00106536
0000204150 Axial muscle weakness, myalgia, diabetes, hypertension, lipodystrophy, coronary artery disease. Muscle biopsy: tubular aggregates, fiber size variability, type I fiber predominance, internal nuclei - TAM-1 Familial, autosomal dominant - - - - - Johann Böhm 00266381
0000204154 Lower limb weakness, myalgia, eye movement defects. Muscle biopsy: tubular aggregates, fiber size variability, internal nuclei, fibrosis - TAM-1 Isolated (sporadic) - - - - - Johann Böhm 00266385
0000207153 - - - Familial, autosomal dominant - - <04y - - Johann Böhm 00269322
0000207793 Upper and lower limb muscle weakness, eye movement defects, contractures - - Familial, autosomal dominant - - - Childhood - Johann Böhm 00271177
0000207794 Lower limb muscle weakness, cramps, eye movement defects, contractures, asplenia, short stature, hypocalcemia, anemia, tooth enamel hypocalcification, - - Isolated (sporadic) - - <10y - - Johann Böhm 00271178
0000351759 Limb-girdle muscular dystrophy * Motor delay * Hyperlordosis * Muscle fiber necrosis * Increased endomysial connective tissue * Abnormal circulating creatine kinase concentration * Specific learning disability LGMD Myopathy, tubular aggregate, 1 Isolated (sporadic) - - - - - Camille Verebi 00466395
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