Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome
1 0 1 0.20 0 0
CUI: C2747824
Disease: Distended bowel
Distended bowel
1 0 1 0.20 0 0
Sudden unexpected nocturnal death syndrome
1 0 1 0.20 0 0
CUI: C3151464
Disease: ATRIAL FIBRILLATION, FAMILIAL, 10
ATRIAL FIBRILLATION, FAMILIAL, 10
1 0 1 0.20 0 0
Wolfram-Like Syndrome, Autosomal Dominant
1 0 1 0.20 0 0
Congenital central diabetes insipidus
1 0 1 0.20 0 0
CUI: C3805412
Disease: CATARACT 41
CATARACT 41
1 0 1 0.20 0 0
CUI: C3808913
Disease: SCHIZOPHRENIA 18
SCHIZOPHRENIA 18
1 0 1 0.20 0 0
Low-frequency sensorineural hearing impairment
1 0 1 0.20 0 0
CUI: C3814825
Disease: Sudden Unexplained Infant Death
Sudden Unexplained Infant Death
1 0 1 0.20 0 0
CUI: C3888911
Disease: CYP2C19 poor metaboliser status
CYP2C19 poor metaboliser status
1 0 1 0.20 0 0
CUI: C4016652
Disease: ATRIAL STANDSTILL 1, DIGENIC
ATRIAL STANDSTILL 1, DIGENIC
1 0 1 0.20 0 0
Complete heart block with broad QRS complexes
1 0 1 0.20 0 0
CUI: C4518338
Disease: Wolfram-like syndrome
Wolfram-like syndrome
1 0 1 0.20 0 0
CUI: C0022890
Disease: Labyrinthine disorder
Labyrinthine disorder
2 0 1 0.17 0 0
CUI: C0036351
Disease: Residual schizophrenia
Residual schizophrenia
2 0 1 0.17 0 0
Other specified conduction disorders
2 0 1 0.17 0 0
CUI: C0235165
Disease: Mania acute
Mania acute
2 0 1 0.17 0 0
CUI: C0235287
Disease: Dysosmia
Dysosmia
2 0 1 0.17 0 0
CUI: C0262548
Disease: maternal hypothyroidism
maternal hypothyroidism
2 0 1 0.17 0 0
CUI: C0340850
Disease: Neurally mediated syncope
Neurally mediated syncope
2 0 1 0.17 0 0
Other specified diabetes mellitus with unspecified complications
2 0 1 0.17 0 0
CUI: C0541782
Disease: Atrial standstill
Atrial standstill
2 0 1 0.17 0 0
CUI: C1096378
Disease: Near sudden infant death syndrome
Near sudden infant death syndrome
2 0 1 0.17 0 0
SICK SINUS SYNDROME 1, AUTOSOMAL RECESSIVE
2 0 1 0.17 0 0