Phenotypes for disease #02591 (CMT2F (Charcot-Marie-Tooth disease, type 2F (CMT-2F)), OMIM:606595)

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     
0000043145 progressive symmetrical weakness, atrophy distal limb muscles initially involving legs particularly peroneal muscles, depressed or absent tendon reflexes, mild/moderate distal sensory abnormalities; age onset 15–25y - - Familial, autosomal dominant - - - - - Johan den Dunnen 00056457
0000043146 Charcot-Marie-Tooth disease, axonal, type 2F - - Familial, autosomal dominant - - - - - Johan den Dunnen 00056458
0000254300 Myalgias, weakness and CK elevation (up to max 3000 U/L), marked calf hypertrophy, negative family history, EMG: pSA and myopathic, muscular biopsy: necrosis and small inflammatory infiltrates (therapy with cortisone, AZA, MTX unsuccessful), / (+) Myopathy,(+) Myalgia,(+) EMG abnormality,(+) EMG: myopathic abnormalities,(+) Necrotizing myopathy,(+) Abnormal skeletal muscle morphology,(+) Pain - - Unknown 44y - - - - Andreas Laner 00359003
0000351591 Fatigable weakness - - Unknown 46y - - - - Andreas Laner 00466208
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