Phenotypes for disease #02795 (LGMDR10;LGMD2J (dystrophy, muscular, limb-girdle, autosomal recessive, type 10 (LGMD2J)), OMIM:608807)

31 entries on 1 page. Showing entries 1 - 31.
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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     
0000044580 severe TMD; IHC no M8/M9-TTN epitopes but A169/A170 normal, CAPN3 severly reduced - - Familial, autosomal dominant - - - - - Johan den Dunnen 00057949
0000044981 - - - - - - - - - Johan den Dunnen 00058350
0000044982 - - - - - - - - - Johan den Dunnen 00058351
0000044983 - - - - - - - - - Johan den Dunnen 00058352
0000044984 - - - - - - - - - Johan den Dunnen 00058353
0000066700 Distal muscle weakness - - Familial, autosomal recessive - - - - - Ana Topf 00087088
0000066765 - - - Familial, autosomal recessive 49y - 44y - - Ana Topf 00087240
0000066766 - - - Familial, autosomal recessive 30y - 25y - - Ana Topf 00087241
0000066767 - - - Familial, autosomal recessive 48y - ? - - Ana Topf 00087243
0000066768 - - - Familial, autosomal recessive 47y - 25y - - Ana Topf 00087245
0000066769 - - - Familial, autosomal recessive 44y - 39y - - Ana Topf 00087247
0000066770 - - - Familial, autosomal recessive 25y - 22y - - Ana Topf 00087248
0000066772 - - - Familial, autosomal recessive 32y - 28y - - Ana Topf 00087250
0000066773 - - - Familial, autosomal recessive 27y - 19y - - Ana Topf 00087251
0000066774 - - - Familial, autosomal recessive 29y - 25y - - Ana Topf 00087252
0000066775 - - - Familial, autosomal recessive 53y - 40y - - Ana Topf 00087253
0000066776 - - - Familial, autosomal recessive 15y - 14y - - Ana Topf 00087254
0000066777 - - - Familial, autosomal recessive 44y - 40y - - Ana Topf 00087244
0000066778 - - - Familial, autosomal recessive 43y - 28y - - Ana Topf 00087255
0000226943 - - - Isolated (sporadic) - - 03y Delayed early motor development - Marco Savarese 00299633
0000226944 Childhood/early-adult onset distal myopathy - - Familial, autosomal recessive - - 08y? Myalgia - Marco Savarese 00299634
0000226945 Childhood/early-adult onset distal myopathy - - Isolated (sporadic) - - 18y? Reduced ankle DF - Marco Savarese 00299635
0000226946 Childhood/early-adult onset distal myopathy - - Familial, autosomal recessive - - 01y? - - Marco Savarese 00299636
0000226947 Childhood/early-adult onset distal myopathy - - Isolated (sporadic) - - - - - Marco Savarese 00299637
0000227499 Childhood/early-adult onset distal myopathy - - Isolated (sporadic) - - 30y? Weakness, muscle pain - Marco Savarese 00300173
0000227501 Childhood/early-adult onset distal myopathy - - Isolated (sporadic) - - 16y? Asymmetrical bilateral foot drop - Marco Savarese 00300174
0000227502 Childhood/early-adult onset distal myopathy - - Isolated (sporadic) - - 20y? Distal lower limb weakness and myoglobinuria - Marco Savarese 00300175
0000227503 Childhood/early-adult onset distal myopathy - - Isolated (sporadic) - - >30y Difficulty in walking - Marco Savarese 00300176
0000227505 hyperCKemia - - Familial, autosomal recessive - - - hyperCKemia - Marco Savarese 00300177
0000250503 Limb-girdle muscular dystrophy HP:0006785 - - Isolated (sporadic) - - - - - Svetlana Gorokhova 00332316
0000274648 delayed motor development; muscular hypotonia; lactic acidosis (Neurological) - LGMD type 2J Familial - - - - - LOVD 00380795
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