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: C0271616
Disease: Precocious female puberty
Precocious female puberty 		1 0 1 0.11 0 0
CUI: C0338650
Disease: Catatonia, Organic
Catatonia, Organic 		1 0 1 0.11 0 0
CUI: C0338900
Disease: Psychasthenic neurosis
Psychasthenic neurosis 		1 0 1 0.11 0 0
CUI: C0342163
Disease: Compensated euthyroidism
Compensated euthyroidism 		1 0 1 0.11 0 0
CUI: C0343560
Disease: Congenital Varicella Syndrome
Congenital Varicella Syndrome 		1 0 1 0.11 0 0
CUI: C0394016
Disease: Coma, Post-Head Injury
Coma, Post-Head Injury 		1 0 1 0.11 0 0
CUI: C0542165
Disease: Pseudoparkinsonism
Pseudoparkinsonism 		1 0 1 0.11 0 0
CUI: C0557875
Disease: Tired
Tired 		1 0 1 0.11 0 0
CUI: C0750993
Disease: Schizophreniform Catatonia
Schizophreniform Catatonia 		1 0 1 0.11 0 0
CUI: C0751812
Disease: Coma, Post-Traumatic, Prolonged
Coma, Post-Traumatic, Prolonged 		1 0 1 0.11 0 0
CUI: C0840564
Disease: Rupture of bladder
Rupture of bladder 		1 0 1 0.11 0 0
CUI: C0848200
Disease: Afterbirth pain
Afterbirth pain 		1 0 1 0.11 0 0
CUI: C0854492
Disease: Tertiary hypothyroidism
Tertiary hypothyroidism 		1 0 1 0.11 0 0
CUI: C0860602
Disease: Anxious personality
Anxious personality 		1 0 1 0.11 0 0
CUI: C1263892
Disease: Neoplasm of cauda equina
Neoplasm of cauda equina 		1 0 1 0.11 0 0
CUI: C1303076
Disease: Tortuous carotid artery
Tortuous carotid artery 		1 0 1 0.11 0 0
CUI: C1527395
Disease: Ogilvie Syndrome
Ogilvie Syndrome 		1 0 1 0.11 0 0
CUI: C1837154
Disease: Drug Metabolism, Poor, CYP2D6-Related
Drug Metabolism, Poor, CYP2D6-Related 		1 0 1 0.11 0 0
CUI: C1960046
Disease: Mild persistent asthma
Mild persistent asthma 		1 0 1 0.11 0 0
CUI: C3280415
Disease: COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA
COGNITIVE IMPAIRMENT WITH OR WITHOUT CEREBELLAR ATAXIA 		1 0 1 0.11 0 0
CUI: C3553418
Disease: PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT
PERIODIC FEVER, MENSTRUAL CYCLE-DEPENDENT 		1 0 1 0.11 0 0
CUI: C3887992
Disease: THYROTROPIN-RELEASING HORMONE DEFICIENCY
THYROTROPIN-RELEASING HORMONE DEFICIENCY 		1 0 1 0.11 0 0
CUI: C3888911
Disease: CYP2C19 poor metaboliser status
CYP2C19 poor metaboliser status 		1 0 1 0.11 0 0
CUI: C4476780
Disease: Reduced amygdala volume
Reduced amygdala volume 		1 0 1 0.11 0 0
CUI: C0085628
Disease: Stupor
Stupor 		2 0 1 1.0E-01 0 0