Phenotypes for disease #03835 (CMS8 (myasthenic syndrome, congenital, type 8, with pre- and postsynaptic defects (CMS-8)), OMIM:615120)

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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     
0000059584 limb-girdle pattern of fatigable muscle weakness with sparing of ocular, facial, bulbar and respiratory muscles - - Familial, autosomal recessive 25y 27y 21y - - Ying Zhang 00079871
0000291836 Peripheral neuropathy (HP:0009830), Decreased nerve conduction velocity (HP:0000762), Bradyphrenia (HP:0031843), Cognitive impairment (HP:0100543), Paresthesia (HP:0003401) Charcot-Marie-Tooth disease - Unknown 59y - 55y Peripheral neuropathy (HP:0009830), Decreased nerve conduction velocity (HP:0000762), Bradyphrenia (HP:0031843), Cognitive impairment (HP:0100543), Paresthesia (HP:0003401) - Yvet den Hartog 00398753
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