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: C1837522
Disease: Impaired pain sensation
Impaired pain sensation
41 0 6 1.0E-01 0 0
CUI: C4021222
Disease: Impaired temperature sensation
Impaired temperature sensation
8 0 3 1.0E-01 0 0
CUI: C1857171
Disease: Episodic hyperhidrosis
Episodic hyperhidrosis
20 0 4 9.8E-02 0 0
CUI: C0030578
Disease: Paronychia Inflammation
Paronychia Inflammation
11 0 3 9.1E-02 0 0
Hereditary Motor and Sensory-Neuropathy Type II
48 0 6 9.0E-02 0 0
CUI: C0349702
Disease: Corneal Scar
Corneal Scar
14 0 3 8.3E-02 0 0
CUI: C1833222
Disease: Autoamputation
Autoamputation
2 0 2 8.0E-02 0 0
CUI: C4024831
Disease: Blotching pigmentation of the skin
Blotching pigmentation of the skin
2 0 2 8.0E-02 0 0
Decreased number of small peripheral myelinated nerve fibers
2 0 2 8.0E-02 0 0
CUI: C4025740
Disease: Autoamputation of foot
Autoamputation of foot
2 0 2 8.0E-02 0 0
CUI: C1838625
Disease: Warburg Sjo Fledelius syndrome
Warburg Sjo Fledelius syndrome
16 0 3 7.9E-02 0 0
CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, AUTOSOMAL DOMINANT
3 0 2 7.7E-02 0 0
CUI: C4025660
Disease: Abnormality of the ankles
Abnormality of the ankles
17 0 3 7.7E-02 0 0
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy
116 0 10 7.6E-02 0 0
CUI: C0010043
Disease: Corneal Ulcer
Corneal Ulcer
33 0 4 7.4E-02 0 0
Absent corpus callosum cataract immunodeficiency
4 0 2 7.4E-02 0 0
CUI: C4025619
Disease: Peripheral axonal atrophy
Peripheral axonal atrophy
4 0 2 7.4E-02 0 0
CUI: C4025722
Disease: Abnormality of the spinal cord
Abnormality of the spinal cord
4 0 2 7.4E-02 0 0
CUI: C0027073
Disease: Myofascial Pain Syndromes
Myofascial Pain Syndromes
5 0 2 7.1E-02 0 0
CUI: C0558844
Disease: Knee reflex absent
Knee reflex absent
5 0 2 7.1E-02 0 0
CUI: C4049342
Disease: Foot osteomyelitis
Foot osteomyelitis
5 0 2 7.1E-02 0 0
CUI: C0013364
Disease: Dysautonomia, Familial
Dysautonomia, Familial
52 0 5 6.9E-02 0 0
CUI: C0236000
Disease: Jaw pain
Jaw pain
6 0 2 6.9E-02 0 0
CUI: C3275447
Disease: Ogden syndrome
Ogden syndrome
6 0 2 6.9E-02 0 0
CUI: C0003892
Disease: Neurogenic arthropathy
Neurogenic arthropathy
7 0 2 6.7E-02 0 0