Phenotypes for disease #03981 (ALS19 (sclerosis, lateral, amyotrophic, type 19 (ALS19)), OMIM:615515)

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     
0000054412 inability to walk (HP:0002540), bulbar (HP:0002483) - - Familial, autosomal dominant - - 70y - - Jamie Zeegers 00074661
0000054413 - - - Familial, autosomal dominant - - 63y - - Jamie Zeegers 00074662
0000054414 upper limb muscle weakness (HP:0003484), no cognitive impairment (-HP:0100543) - - Familial, autosomal dominant - - 63y - - Jamie Zeegers 00074663
0000054415 respiration (HP:0004347) - - Familial, autosomal dominant - - 60y - - Jamie Zeegers 00074664
0000054416 upper limb muscle weakness (HP:0003484), slow progression (HP:0003677) - - Familial, autosomal dominant - - 67y - - Jamie Zeegers 00074665
0000054417 upper limb muscle weakness (HP:0003484) - - Isolated (sporadic) - - 45y - - Jamie Zeegers 00074666
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