Symptom Information: Sort according to HPO 

1
(HPO:0009830) Peripheral neuropathy Very frequent [Orphanet] 206 / 7739
2
(HPO:0003202) Skeletal muscle atrophy Very frequent [Orphanet] 281 / 7739
3
(HPO:0001761) Pes cavus Very frequent [Orphanet] 225 / 7739
4
(HPO:0002808) Kyphosis Occasional [Orphanet] 289 / 7739
5
(HPO:0003134) Abnormality of peripheral nerve conduction Very frequent [Orphanet] 38 / 7739
6
(HPO:0001337) Tremor Occasional [Orphanet] 200 / 7739
7
(HPO:0001288) Gait disturbance Occasional [Orphanet] 318 / 7739
8
(HPO:0004374) Hemiplegia/hemiparesis Occasional [Orphanet] 158 / 7739
9
(HPO:0010488) Aplasia/Hypoplasia of the palmar creases Very frequent [Orphanet] 15 / 7739
10
(HPO:0001284) Areflexia 198 / 7739
11
(HPO:0001315) Reduced tendon reflexes Very frequent [Orphanet] 160 / 7739
12
(HPO:0001324) Muscle weakness Very frequent [Orphanet] 859 / 7739
13
(HPO:0002066) Gait ataxia Occasional [Orphanet] 327 / 7739
14
(HPO:0007021) Pain insensitivity Frequent [Orphanet] 35 / 7739
15
(HPO:0002650) Scoliosis Occasional [Orphanet] 705 / 7739
16
(HPO:0001249) Intellectual disability Rare [HPO:probinson] 1089 / 7739
17
(HPO:0002167) Neurological speech impairment Occasional [Orphanet] 308 / 7739
18
(HPO:0002460) Distal muscle weakness 122 / 7739
19
(HPO:0002936) Distal sensory impairment 96 / 7739
20
(HPO:0003376) Steppage gait 41 / 7739
21
(HPO:0003431) Decreased motor nerve conduction velocity 51 / 7739
22
(HPO:0003482) EMG: axonal abnormality 3 / 7739
23
(HPO:0003484) Upper limb muscle weakness 19 / 7739
24
(HPO:0003693) Distal amyotrophy Rare [HPO:probinson] 118 / 7739
25
(HPO:0009027) Foot dorsiflexor weakness 45 / 7739
26
(OMIM) Mental retardation has been reported 3 / 7739
27
(OMIM) Distal muscle weakness due to peripheral neuropathy 4 / 7739
28
(OMIM) Distal muscle atrophy due to peripheral neuropathy 2 / 7739
29
(OMIM) Mild to moderate distal sensory impairment 2 / 7739
30
(OMIM) Decreased nerve conduction velocities (NCV), suggesting demyelination 2 / 7739
31
(OMIM) EMG findings suggest axonal involvement 2 / 7739
32
(OMIM) Upper limb involvement may occur later 10 / 7739
33
(HPO:0002360) Sleep disturbance Occasional [Orphanet] 113 / 7739
34
(HPO:0003474) Sensory impairment Very frequent [Orphanet] 54 / 7739
35
(HPO:0011442) Abnormality of central motor function Frequent [Orphanet] 76 / 7739
36
(HPO:0012758) Neurodevelopmental delay Frequent [Orphanet] 949 / 7739
37
(HPO:0001419) X-linked recessive inheritance 189 / 7739
38
(HPO:0003593) Infantile onset 249 / 7739