Phenotypes for disease #02705 (RMD2;LGMD1C (rippling muscle disease, type 2 (LGMD1C)), OMIM:607801)

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000228654 - - - Familial, autosomal dominant - - - - - Helen Latsoudis 00301523
0000235209 Proximal muscle weakness of lower limbs (HP:0008994), Toe walking (HP:0040083), Frequent falls (HP:0002527), Myalgia (HP:0003326), Gowers sign (HP:0003391), Hyperlordosis (HP:0003307), Calf muscle pseudohypertrophy (HP:0003707), Flexion contracture (HP:0001371), Elevated serum creatinine kinase (HP:0003236), EMG abnormality (HP:0003457) Dystrophinopathy LGMD1C Isolated (sporadic) 08y 08y 02y06m Proximal muscle weakness of lower limbs (HP:0008994) - Mehwish Zehravi 00309878
0000235511 Muscle weakness (HP:0001324), Progressive muscle weakness (HP:0003323),Difficulty climbing stairs (HP:0003551), Difficulty walking (HP:0002355), Toe walking (HP:0040083), Frequent falls (HP:0002527), Myalgia (HP:0003326), Gowers sign (HP:0003391), Hyperlordosis (HP:0003307), Calf muscle pseudohypertrophy (HP:0003707), Flexion contracture (HP:0001371), Elevated serum creatinine kinase (HP:0003236), EMG abnormality (HP:0003457) DMD/ LGMD LGMD1C Isolated (sporadic) 12y 12y 05y Gowers sign (HP:0003391) - Mehwish Zehravi 00310208
0000257382 Hypotonia HP:0001252 - - Isolated (sporadic) - - - - - Ibrahim Sahin 00361989
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