Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Hereditary Sensory Autonomic Neuropathy, Type 1
32 0 4 0.12 0 0
CUI: C0234250
Disease: Pain, Referred
Pain, Referred
4 0 1 0.11 0 0
CUI: C0522187
Disease: Tocophobia
Tocophobia
4 0 1 0.11 0 0
CUI: C0948595
Disease: Ocular discomfort
Ocular discomfort
4 0 1 0.11 0 0
CUI: C2902981
Disease: Neurogenic bladder dysfunction
Neurogenic bladder dysfunction
4 0 1 0.11 0 0
CUI: C3662528
Disease: Discogenic pain
Discogenic pain
4 0 1 0.11 0 0
CUI: C4025619
Disease: Peripheral axonal atrophy
Peripheral axonal atrophy
4 0 1 0.11 0 0
CUI: C0027073
Disease: Myofascial Pain Syndromes
Myofascial Pain Syndromes
5 0 1 1.0E-01 0 0
CUI: C0268849
Disease: Overactive Detrusor
Overactive Detrusor
5 0 1 1.0E-01 0 0
CUI: C0741548
Disease: bladder symptoms
bladder symptoms
5 0 1 1.0E-01 0 0
CUI: C1868702
Disease: Diabetic keratopathy
Diabetic keratopathy
5 0 1 1.0E-01 0 0
CUI: C4021578
Disease: Chronic axonal neuropathy
Chronic axonal neuropathy
5 0 1 1.0E-01 0 0
CUI: C0231791
Disease: Toeing-in
Toeing-in
6 0 1 9.1E-02 0 0
CUI: C0236000
Disease: Jaw pain
Jaw pain
6 0 1 9.1E-02 0 0
CUI: C0406670
Disease: Vulvodynia
Vulvodynia
6 0 1 9.1E-02 0 0
Myopathy, Centronuclear, Autosomal Recessive
6 0 1 9.1E-02 0 0
Multiple self-healing squamous epithelioma
6 0 1 9.1E-02 0 0
CUI: C0579144
Disease: Cavovarus deformity of foot
Cavovarus deformity of foot
6 0 1 9.1E-02 0 0
CUI: C0796037
Disease: Martsolf syndrome
Martsolf syndrome
6 0 1 9.1E-02 0 0
CUI: C1262037
Disease: Diabetic cystopathy
Diabetic cystopathy
6 0 1 9.1E-02 0 0
CUI: C4479708
Disease: FCD IIA
FCD IIA
6 0 1 9.1E-02 0 0
CUI: C0043208
Disease: Wolman Disease
Wolman Disease
19 0 2 8.7E-02 0 0
Hereditary Sensory Autonomic Neuropathy, Type 5
7 0 1 8.3E-02 0 0
CUI: C0238015
Disease: Autonomic Dysreflexia
Autonomic Dysreflexia
7 0 1 8.3E-02 0 0
CUI: C0271682
Disease: Mixed sensory-motor polyneuropathy
Mixed sensory-motor polyneuropathy
20 0 2 8.3E-02 0 0