Phenotypes for disease #00456 (ALS1 (sclerosis, lateral, amyotrophic, type 1 (ALS1)), OMIM:105400)

6 entries on 1 page. Showing entries 1 - 6.
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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     
0000016230 age onset 67y progressive muscle atrophy, weakness in all extremities, postural tremor upper extremities; 68y diffuse muscle atrophy, weakness, fasciculation, hyporeflexia all extremities., weakness neck flexion, normal intelligence was normal, no bulbar sign nor pyramidal sign, EMG diffuse active neurogenic changes - - Isolated (sporadic) 68y - - - - Johan den Dunnen 00017872
0000016231 see paper - - Familial - - - - - Johan den Dunnen 00017873
0000016233 see paper - - Familial - - - - - Johan den Dunnen 00017876
0000016234 see paper - - Isolated (sporadic) - - - - - Johan den Dunnen 00017877
0000016235 see paper - - Isolated (sporadic) - - - - - Johan den Dunnen 00017878
0000060647 Amyotrophic lateral sclerosis, susceptibility to (OMIM:105400) - - Familial, autosomal dominant - - - - - Daniel Trujillano 00081078
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