Phenotypes for disease #02565 (NM;IBM2 (myopathy, Nonaka (NM, inclusion body myopathy, type 2 (IBM-2))), OMIM:605820)

16 entries on 1 page. Showing entries 1 - 16.
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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     
0000042728 myopathy, Nonaka; - - Isolated (sporadic) - - 21y - - Johan den Dunnen 00056090
0000042729 myopathy, Nonaka; moderate proximal weakness L/E, quadriceps involvement, atrophy hand muscles; - - Unknown - - 25y - - Johan den Dunnen 00056091
0000042730 myopathy, Nonaka, typical; - - Isolated (sporadic) - - 25y - - Johan den Dunnen 00056092
0000042731 myopathy, Nonaka, typical; - - Isolated (sporadic) - - 33y - - Johan den Dunnen 00056093
0000042732 myopathy, Nonaka, typical; - - Isolated (sporadic) - - 24y - - Johan den Dunnen 00056094
0000042733 myopathy, Nonaka, typical; - - Isolated (sporadic) - - 18y - - Johan den Dunnen 00056095
0000042734 myopathy, Nonaka, typical; - - Familial - - 15y - - Johan den Dunnen 00056096
0000042735 myopathy, Nonaka; late onset, slowly progressive; - - Unknown - - 40y - - Johan den Dunnen 00056097
0000042736 myopathy, Nonaka, typical; - - Familial - - 25y - - Johan den Dunnen 00056098
0000042737 myopathy, Nonaka; - - Isolated (sporadic) - - 24y - - Johan den Dunnen 00056099
0000042768 myopathy, Nonaka; CPK 2281 - - Familial - - 26y - - Johan den Dunnen 00056130
0000082788 - - - Familial, autosomal recessive - - - - - Satomi Mitsuhashi 00104895
0000125745 see paper; ..., myopathy, thrombocytopenia (during treatment for neonatal jaundice) myopathy GNE myopathy Familial, autosomal recessive 32y - - - - Johan den Dunnen 00153017
0000299787 see paper; ..., weakness of foot dorsal/plantar flexors and hamstrings, leg atrophy, pes cavus; CK level normal; CT fatty change in the gastrocnemius > tibialis anterior, biceps femoris and gluteus medius muscles bilaterally; muscle biopsy internalized nuclei, fiber type grouping; slow progression of weakness; >15y-ambulatory without aid motor axonal neuropathy NM Familial, autosomal recessive 50y - 48y - - Johan den Dunnen 00248389
0000299788 asymetric weakness of foot dorsiflexors and hamstring, unilateral interossei and wrist extensors/flexors, atrophy of weak muscles; raised CK (900U/L); MRI fatty change in the tibialis anterior, medial gastrocnemius and semitendinosus muscles; STIR hyperintensity of tibialis anterior; diffuse limb fasciculations after 6m, progression of weakness after 1 y motor axonal neuropathy NM Familial, autosomal recessive 34y - 33y - - Johan den Dunnen 00407641
0000299789 asymetric weakness foot dorsiflexors, bilateral Achilles’ tendon retraction; normal CK; CT fatty change, atrophy tibialis anterior bilaterally; muscle biopsy fiber type grouping angular atrophic fibers (one with rimmed vacuoles), nuclear clumps; slow progression weakness, involvement of distal upper limb muscles; 19y-ambulatory with aid motor axonal neuropathy NM Familial, autosomal recessive 54y - 41y - - Johan den Dunnen 00407642
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