Source: ALL
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: C0013124
Disease: Drinking behavior processes
Drinking behavior processes 		0 31 0 0 1 3.3E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 3.6E-03
CUI: C0152194
Disease: Irregular astigmatism
Irregular astigmatism 		0 1 0 0 1 3.6E-03
CUI: C0233689
Disease: Delusion of infidelity
Delusion of infidelity 		0 1 0 0 1 3.6E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 3.5E-03
CUI: C0268503
Disease: Autosomal recessive ocular albinism
Autosomal recessive ocular albinism 		0 4 0 0 1 3.6E-03
CUI: C0271681
Disease: Sensory polyneuropathy
Sensory polyneuropathy 		0 1 0 0 1 3.6E-03
CUI: C0678189
Disease: Hyperlipidemia, group A
Hyperlipidemia, group A 		0 1 0 0 1 3.6E-03
CUI: C0702157
Disease: Thalassemia trait
Thalassemia trait 		0 2 0 0 2 7.2E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 3.6E-03
CUI: C0752138
Disease: Intracranial Arterial Diseases
Intracranial Arterial Diseases 		0 1 0 0 1 3.6E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 3.6E-03
CUI: C1095928
Disease: Secondary hyperthyroidism
Secondary hyperthyroidism 		0 1 0 0 1 3.6E-03
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		0 1 0 0 1 3.6E-03
CUI: C1511306
Disease: Breast Diffuse Large B-Cell Lymphoma
Breast Diffuse Large B-Cell Lymphoma 		0 1 0 0 1 3.6E-03
CUI: C1721007
Disease: Pachyonychia Congenita, Type 2 (disorder)
Pachyonychia Congenita, Type 2 (disorder) 		0 13 0 0 2 7.0E-03
CUI: C1847024
Disease: ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder)
ALBINISM, OCULOCUTANEOUS, TYPE IB (disorder) 		0 24 0 0 1 3.3E-03
CUI: C1847132
Disease: ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE
ALBINISM, OCULOCUTANEOUS, TYPE I, TEMPERATURE-SENSITIVE 		0 2 0 0 1 3.6E-03
CUI: C1861678
Disease: Charcot-Marie-Tooth Disease, Axonal, Type 2a1
Charcot-Marie-Tooth Disease, Axonal, Type 2a1 		0 1 0 0 1 3.6E-03
CUI: C1963757
Disease: Dopamine dysregulation syndrome
Dopamine dysregulation syndrome 		0 1 0 0 1 3.6E-03
CUI: C2608086
Disease: HANGOVER, SUSCEPTIBILITY TO (finding)
HANGOVER, SUSCEPTIBILITY TO (finding) 		0 1 0 0 1 3.6E-03
CUI: C2676227
Disease: SUBLINGUAL NITROGLYCERIN, SUSCEPTIBILITY TO POOR RESPONSE TO
SUBLINGUAL NITROGLYCERIN, SUSCEPTIBILITY TO POOR RESPONSE TO 		0 1 0 0 1 3.6E-03
CUI: C2677190
Disease: SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 3 (disorder)
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 3 (disorder) 		0 13 0 0 1 3.5E-03
CUI: C2677821
Disease: Prostate Cancer, Hereditary, 13
Prostate Cancer, Hereditary, 13 		0 1 0 0 1 3.6E-03
CUI: C3149136
Disease: SKIN/HAIR/EYE PIGMENTATION 3, BLUE/GREEN EYES
SKIN/HAIR/EYE PIGMENTATION 3, BLUE/GREEN EYES 		0 1 0 0 1 3.6E-03