Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C4721916
Disease: HMSN Type V
HMSN Type V
7 0 7 0.26 0 0
Urinary bladder sphincter dysfunction
28 0 9 0.20 0 0
Spastic paraplegia 10, autosomal dominant
16 0 7 0.19 0 0
Impaired vibration sensation in the lower limbs
39 0 10 0.18 0 0
CUI: C0085606
Disease: Urgency of micturition
Urgency of micturition
40 0 10 0.18 0 0
CUI: C4553976
Disease: Urinary Urgency, CTCAE 5
Urinary Urgency, CTCAE 5
34 0 9 0.17 0 0
CUI: C0231687
Disease: Spastic gait
Spastic gait
62 0 13 0.17 0 0
CUI: C1271100
Disease: Lower limb spasticity
Lower limb spasticity
43 0 10 0.17 0 0
CUI: C1843175
Disease: Hyperreflexia in upper limbs
Hyperreflexia in upper limbs
16 0 6 0.16 0 0
CUI: C0393555
Disease: Pure hereditary spastic paraplegia
Pure hereditary spastic paraplegia
9 0 5 0.16 0 0
CUI: C0238651
Disease: Ankle clonus
Ankle clonus
32 0 8 0.16 0 0
Spastic paraplegia 4, autosomal dominant
10 101 5 0.16 2 1.9E-02
Autosomal Recessive Hereditary Spastic Paraplegia
20 0 6 0.15 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary
123 41 19 0.15 1 2.1E-02
X-Linked, Spastic Paraplegia, Hereditary
5 0 4 0.14 0 0
CUI: C1389102
Disease: Atrophy of the spinal cord
Atrophy of the spinal cord
13 0 5 0.14 0 0
Degeneration of the lateral corticospinal tracts
21 0 6 0.14 0 0
CUI: C1836696
Disease: Lower limb hyperreflexia
Lower limb hyperreflexia
38 0 8 0.14 0 0
CUI: C1836296
Disease: Muscle Weakness Lower Limb
Muscle Weakness Lower Limb
74 0 12 0.13 0 0
CUI: C1846017
Disease: Progressive pes cavus
Progressive pes cavus
9 0 4 0.12 0 0
Hereditary X-Linked Recessive Spastic Paraplegia
10 0 4 0.12 0 0
CUI: C2931276
Disease: Spastic paraplegia 17
Spastic paraplegia 17
12 0 4 0.11 0 0
Spastic paraplegia 3, autosomal dominant
3 18 3 0.11 1 4.2E-02
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia
144 93 16 0.10 2 2.0E-02
SPASTIC PARAPLEGIA 7, AUTOSOMAL RECESSIVE
6 0 3 1.0E-01 0 0