Symptom Information: Sort according to HPO 

1
(HPO:0001284) Areflexia 15372378 IBIS 198 / 7739
2
(HPO:0002015) Dysphagia 11/24 [HPO:probinson] 15372378 IBIS 301 / 7739
3
(HPO:0002062) Morphological abnormality of the pyramidal tract 15372378 IBIS 24 / 7739
4
(HPO:0002174) Postural tremor 15372378 IBIS 22 / 7739
5
(HPO:0002380) Fasciculations 23/24 [HPO:probinson] 15372378 IBIS 42 / 7739
6
(HPO:0002460) Distal muscle weakness 10/24 [HPO:probinson] 15372378 IBIS 122 / 7739
7
(HPO:0002529) Neuronal loss in central nervous system 15372378 IBIS 37 / 7739
8
(HPO:0003202) Skeletal muscle atrophy 15372378 IBIS 281 / 7739
9
(HPO:0003323) Progressive muscle weakness 15372378 IBIS 17 / 7739
10
(HPO:0003394) Muscle cramps 21/23 [HPO:probinson] 15372378 IBIS 106 / 7739
11
(HPO:0003701) Proximal muscle weakness 19/24 [HPO:probinson] 15372378 IBIS 105 / 7739
12
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739
13
(HPO:0001260) Dysarthria 329 / 7739
14
(HPO:0007354) Amyotrophic lateral sclerosis 25 / 7739