Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
HUNTINGTON DISEASE-LIKE 3 (disorder)
2 0 1 0.50 0 0
CUI: C3875011
Disease: Familial hyperalphalipoproteinemia
Familial hyperalphalipoproteinemia
5 0 1 0.20 0 0
CUI: C1858116
Disease: Caudate atrophy
Caudate atrophy
6 0 1 0.17 0 0
CUI: C4025360
Disease: Functional motor deficit
Functional motor deficit
10 0 1 1.0E-01 0 0
Headache associated with sexual activity
14 0 1 7.1E-02 0 0
CUI: C0422895
Disease: Primitive reflex
Primitive reflex
14 0 1 7.1E-02 0 0
Primitive reflexes (palmomental, snout, glabellar)
14 0 1 7.1E-02 0 0
CUI: C0376286
Disease: Avitaminosis
Avitaminosis
17 0 1 5.9E-02 0 0
CUI: C1510471
Disease: Vitamin Deficiency
Vitamin Deficiency
17 0 1 5.9E-02 0 0
CUI: C1853578
Disease: Neuroferritinopathy
Neuroferritinopathy
17 0 1 5.9E-02 0 0
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial
18 0 1 5.6E-02 0 0
CUI: C1847987
Disease: HUNTINGTON DISEASE-LIKE 2
HUNTINGTON DISEASE-LIKE 2
18 0 1 5.6E-02 0 0
CUI: C0155210
Disease: Eyelid Xanthoma
Eyelid Xanthoma
19 0 1 5.3E-02 0 0
CUI: C3494652
Disease: Severe dementia
Severe dementia
19 0 1 5.3E-02 0 0
CUI: C0020597
Disease: Hypobetalipoproteinemias
Hypobetalipoproteinemias
20 0 1 5.0E-02 0 0
CUI: C0473527
Disease: Hypoalphalipoproteinemias
Hypoalphalipoproteinemias
20 0 1 5.0E-02 0 0
CUI: C1846707
Disease: SPINOCEREBELLAR ATAXIA 17
SPINOCEREBELLAR ATAXIA 17
28 0 1 3.6E-02 0 0
CUI: C0302314
Disease: Xanthoma
Xanthoma
29 0 1 3.4E-02 0 0
CUI: C0393576
Disease: Chorea Acanthocytosis Syndrome
Chorea Acanthocytosis Syndrome
29 0 1 3.4E-02 0 0
CUI: C0240735
Disease: Personality Change
Personality Change
43 0 1 2.3E-02 0 0
Serum gamma-glutamyl transferase measurement
54 0 1 1.9E-02 0 0
CUI: C2936179
Disease: Obesity, Visceral
Obesity, Visceral
55 0 1 1.8E-02 0 0
CUI: C0011253
Disease: Delusions
Delusions
62 0 1 1.6E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 1.5E-02 0 0
CUI: C0752121
Disease: Spinocerebellar Ataxia Type 2
Spinocerebellar Ataxia Type 2
76 0 1 1.3E-02 0 0