Phenotypes for disease #05652 (LGMDR23 (dystrophy, muscular, limb-girdle, autosomal recessive, type 23 (LGMDR-23)), OMIM:618138)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Diagnosis/Initial     

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Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

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Individual ID     
0000228715 - - - Familial, autosomal recessive - - - - Helen Latsoudis 00301610
0000308417 - - Elevated circulating creatine kinase concentration, Proximal muscle weakness, Hyporeflexia, Seizure; (CK elevation as incidental finding in clarification after seizure, differential diagnosis aspiration event/bolus event. Values between 800 and 1000 U/L, mild proximal muscle weakness, hypo-/reflexia.) Unknown 02y - - - Andreas Laner 00416905
0000335626 - LGMDR23 (# 618138) HP:0011463 Childhood onset No Seizure Ambulant (7 years old) Familial, autosomal recessive - - 02y - María Eugenia Foncuberta 00446401
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