Phenotypes for disease #01944 (LGMDR5;LGMD2C (dystrophy, muscular, limb-girdle, autosomal recessive, type 5 (LGMD2C)), OMIM:253700)

20 entries on 1 page. Showing entries 1 - 20.
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Individual ID     
0000051911 proximal muscle weakness (HP:0003701), no motor delay (-HP:0001270), no cognitive impairment (-HP:0100543), no ambulation (-HP:0002540), bilateral calf hypertrophy (HP:0008981), mild scapular winging (HP:0003691), no joint contractures (-HP:0001371) - - Familial, autosomal recessive - - 06y - - Jamie Zeegers 00072206
0000051912 proximal muscle weakness (HP:0003701), no ambulation (-HP:0002540), bilateral calf hypertrophy (HP:0008981), mild scapular winging (HP:0003691), no joint contractures (-HP:0001371), pelvic girdle muscles weakness (HP:0003749), lordosis (HP:0003307), waddling gait (HP:0002515), macroglossia (HP:0000158), no facial weakness (-HP:0010628) - - Familial, autosomal recessive - - 09y - - Jamie Zeegers 00072208
0000106030 clinical grade V; elevated CPK (HP:0003236); >17y-inable to walk (HP:0002540) severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Isolated (sporadic) - 7y 7y difficulty climbing stairs/running IHC/WB SGCA trace Johan den Dunnen 00133283
0000106045 clinical grade VI/VII; 21y-inable to walk (HP:0002540) severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Isolated (sporadic) - 8y 8y difficulty climbing stairs/running IHC SGCA trace, SGC weak, SSPN weak; WB SGCA trace Johan den Dunnen 00133298
0000106046 clinical grade III; >26y-inable to walk (HP:0002540) severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Isolated (sporadic) - 12y 14y difficulty climbing stairs/running IHC/WB SGCA weak; IHC SGC weak, SSPN weak Johan den Dunnen 00133299
0000106048 13y-inable to walk (HP:0002540) severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Isolated (sporadic) - 9y - - - Johan den Dunnen 00133301
0000106056 severe (clinical grade VII), walk tip-toe; 22y-inable to walk (HP:0002540) severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Isolated (sporadic) - 9y 6y difficulty climbing stairs/running IHC/WB no SGCA Johan den Dunnen 00133309
0000106100 clinical grade IV, walk tip-toe; >36y-inable to walk (HP:0002540) severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Isolated (sporadic) - 9y 6y difficulty climbing stairs/running IHC/WB SGCA weak Johan den Dunnen 00133353
0000106113 - severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Isolated (sporadic) - - - - IHC SGC weak, SSPN weak Johan den Dunnen 00133366
0000106117 severe; 22y-inable to walk (HP:0002540)/10y-inable to walk (HP:0002540)- severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Isolated (sporadic) - 07y-09y - - - Johan den Dunnen 00133370
0000106120 clinical grade III; >25y-inable to walk (HP:0002540) severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Isolated (sporadic) - 12y 13y difficulty climbing stairs/running IHC SGCA weak, WB SGCA trace Johan den Dunnen 00133373
0000106133 1108 elevated CPK (HP:0003236) severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Unknown - - 15y - - Johan den Dunnen 00133386
0000106134 clinical grade III; >31y-inable to walk (HP:0002540) severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Familial - 15y - exercise intolerance IHC SGC weak, SSPN weak Johan den Dunnen 00133387
0000106135 clinical grade III; >33y-inable to walk (HP:0002540) severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Familial - 12y - exercise intolerance IHC SGCA weak, WB SGCA reduced Johan den Dunnen 00133388
0000106138 severe (clinical grade VII), walk tip-toe; 14y-inable to walk (HP:0002540) severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Isolated (sporadic) - 6y 6y difficulty climbing stairs/running IHC no SGCA, WB SGCA trace Johan den Dunnen 00133391
0000106219 severe (clinical grade VII), walk tip-toe; 13y-inable to walk (HP:0002540) severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Isolated (sporadic) - 6y 6y difficulty climbing stairs/running IHC no SGCA, IHC SGC weak, SSPN weak; WB SGCA trace Johan den Dunnen 00133472
0000106258 - severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Familial - - - - - Marina Fanin 00133511
0000106260 - severe autosomal recessive muscular dystrophy, North African type (SCARMD) - Unknown - - - - WB reduced SGCA Marina Fanin 00133513
0000161574 Suspected Duchenne muscular dystrophy, but with normal results on multiplex PCR and MLPA for DMD gene Suspected Duchenne muscular dystrophy Limb-girdle muscular dystrophy type 2C (LGMD2C) Familial, autosomal recessive 08y - ? Muscular dystrophy No muscle biopsy performed Miguel Angel Alcántara-Ortigoza 00213094
0000322150 Elevated circulating creatine kinase concentration, Muscle atrophy - - Familial, autosomal recessive 06y - - - - Andreas Laner 00431575
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