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: C0699739
Disease: Sensory Neuropathy, Hereditary
Sensory Neuropathy, Hereditary
19 0 11 0.33 0 0
Hereditary Sensory Autonomic Neuropathy, Type 1
32 14 12 0.27 3 0.18
CUI: C0002768
Disease: Congenital Pain Insensitivity
Congenital Pain Insensitivity
14 0 8 0.26 0 0
Hereditary Sensory Autonomic Neuropathy, Type 2
8 0 6 0.22 0 0
Hereditary Sensory Radicular Neuropathy
5 0 5 0.20 0 0
Indifference to Pain, Congenital, Autosomal Recessive
23 0 8 0.20 0 0
Hereditary Sensory Autonomic Neuropathy, Type 5
7 0 5 0.19 0 0
CUI: C1837602
Disease: Painless fractures due to injury
Painless fractures due to injury
8 0 5 0.18 0 0
CUI: C4732740
Disease: Acral ulceration
Acral ulceration
8 0 5 0.18 0 0
CUI: C0151934
Disease: Hypogeusia
Hypogeusia
6 0 4 0.15 0 0
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2B (disorder)
6 0 4 0.15 0 0
CUI: C0151572
Disease: Reflex, Corneal, Decreased
Reflex, Corneal, Decreased
14 0 5 0.15 0 0
Decreased sensory nerve conduction velocity
15 0 5 0.14 0 0
CUI: C1852289
Disease: Autoamputation of digits
Autoamputation of digits
8 0 4 0.14 0 0
CUI: C0020074
Disease: HSAN Type IV
HSAN Type IV
9 0 4 0.13 0 0
Distal sensory impairment of all modalities
9 0 4 0.13 0 0
CUI: C4025676
Disease: Abnormality of the knee
Abnormality of the knee
10 0 4 0.13 0 0
Decreased number of peripheral myelinated nerve fibers
28 0 6 0.13 0 0
CUI: C0003028
Disease: Anhidrosis
Anhidrosis
37 0 7 0.13 0 0
CUI: C0259749
Disease: Autonomic neuropathy
Autonomic neuropathy
29 0 6 0.12 0 0
CUI: C0344307
Disease: Absence of pain sensation
Absence of pain sensation
14 0 4 0.11 0 0
Neuropathy, Hereditary Sensory And Autonomic, Type IIA
5 0 3 0.11 0 0
CUI: C0917990
Disease: Acro-Osteolysis
Acro-Osteolysis
16 0 4 0.11 0 0
CUI: C4025744
Disease: Foot acroosteolysis
Foot acroosteolysis
6 0 3 0.11 0 0
CUI: C1833225
Disease: Dystrophic toenail
Dystrophic toenail
18 0 4 0.10 0 0