Phenotypes for disease #01452 (SMAPME (atrophy, muscular, spinal, with progressive myoclonic epilepsy), OMIM:159950)

10 entries on 1 page. Showing entries 1 - 10.
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AscendingPhenotype ID     

Phenotype details     

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Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

Age/Onset     

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Individual ID     
0000044435 normal early development, progressive muscle weakness; 10y-brief episodes unconsciousness, myoclonic jerks; 11y-diffuse muscle atrophy - - Isolated (sporadic) - - 5y muscle weakness - Johan den Dunnen 00057784
0000044438 proximal weakness, muscular atrophy; EMG chronic denervation; 7y-brief myoclonic seizures; CPK: normal; w14m - - Isolated (sporadic) - - 5y walking difficulties, frequent falls, tremor hands - Johan den Dunnen 00057787
0000044439 myoclonic epilepsy, muscle weakness from chronic denervation; CPK: normal - - Isolated (sporadic) - - - - - Johan den Dunnen 00057788
0000044440 myoclonic epilepsy, muscle weakness from chronic denervation; CPK: normal - - Isolated (sporadic) - - - - - Johan den Dunnen 00057789
0000044441 normal motor/intellectual milestones, progressive muscle weakness (lower then upper limbs); 12y-generalized epileptic seizures, numerous brief episodes unconsciousness, myoclonic jerks - - Isolated (sporadic) - - 4y muscle weakness - Johan den Dunnen 00057790
0000044442 normal motor/intellectual milestones, progressive muscle weakness (lower then upper limbs); 12y-generalized epileptic seizures, numerous brief episodes unconsciousness, myoclonic jerks - - Isolated (sporadic) - - 5y muscle weakness - Johan den Dunnen 00057791
0000128881 - - - Familial, autosomal recessive 24y - - - - Gisèle Bonne 00163649
0000254808 (+) Ataxia,(+) Global developmental delay,(+) Profound global developmental delay,(+) Epileptic encephalopathy,(+) Akathisia - - Familial, autosomal recessive 04y - - - - Andreas Laner 00359554
0000257428 Onset age 10 of multifocal action and rest myoclonus, on a background of normal development and early severe hearing impairment (4y) . Subsequent progressive limb and bulbar weakness, tonic-clonic seiures (16 yr) and late cognitive decline. Rapidly progressive, death age 19. Unverricht-Lundborg disease like - Familial, autosomal recessive - - - - - Johan den Dunnen 00334911
0000352768 see paper; ..., moderate; no hoarseness of voice; no joint pain, no joint contractures; no subcutaneous nodules; no pulmonary disease, no cardiac disease; no organomegaly; normal fundus; developmental delay, seizures spinal muscle atrophy with progressive myoclonic epilepsy SMAPME Familial, autosomal recessive - - - - - Johan den Dunnen 00301412
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