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 and idiopathic neuropathy, unspecified
0 6 0 0 1 3.4E-02
NEUROPATHY, CONGENITAL HYPOMYELINATING, 3
0 13 0 0 1 2.8E-02
CUI: C0001889
Disease: Akinetic Mutism
Akinetic Mutism
1 0 1 2.4E-02 0 0
CUI: C0016512
Disease: Foot pain
Foot pain
1 0 1 2.4E-02 0 0
CUI: C0022802
Disease: Kuru
Kuru
1 0 1 2.4E-02 0 0
CUI: C0040416
Disease: Tonic Pupil
Tonic Pupil
1 0 1 2.4E-02 0 0
CUI: C0151772
Disease: Manic psychosis
Manic psychosis
1 0 1 2.4E-02 0 0
Nystagmus associated with disorder of the vestibular system
1 0 1 2.4E-02 0 0
CUI: C0233623
Disease: Onychotillomania
Onychotillomania
1 0 1 2.4E-02 0 0
CUI: C0234244
Disease: Tissue Pain
Tissue Pain
1 0 1 2.4E-02 0 0
CUI: C0235198
Disease: Unable to concentrate
Unable to concentrate
1 0 1 2.4E-02 0 0
CUI: C0236960
Disease: Dementia due to Parkinson's disease
Dementia due to Parkinson's disease
1 0 1 2.4E-02 0 0
Osteoarthropathy of fingers familial
1 0 1 2.4E-02 0 0
Spondylometaphyseal dysplasia, Kozlowski type
1 0 1 2.4E-02 0 0
CUI: C0265281
Disease: Metatropic dwarfism
Metatropic dwarfism
1 0 1 2.4E-02 0 0
CUI: C0333157
Disease: Colloid Cysts
Colloid Cysts
1 0 1 2.4E-02 0 0
CUI: C0334346
Disease: Apocrine adenocarcinoma
Apocrine adenocarcinoma
1 0 1 2.4E-02 0 0
Noninfiltrating intraductal papillary adenocarcinoma
1 0 1 2.4E-02 0 0
Hereditary cerebrovascular amyloidosis
1 0 1 2.4E-02 0 0
CUI: C0422879
Disease: CNS symptom
CNS symptom
1 0 1 2.4E-02 0 0
CUI: C0432227
Disease: Brachyolmia Type 3
Brachyolmia Type 3
1 0 1 2.4E-02 0 0
CUI: C0562557
Disease: Sexually disinhibited behavior
Sexually disinhibited behavior
1 0 1 2.4E-02 0 0
CUI: C0679441
Disease: Disorder of olfactory system
Disorder of olfactory system
1 0 1 2.4E-02 0 0
CUI: C0742115
Disease: Cerebritis
Cerebritis
1 0 1 2.4E-02 0 0
CUI: C0748375
Disease: retinal neuropathy
retinal neuropathy
1 0 1 2.4E-02 0 0