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: C1970187
Disease: Deafness, Sensorineural, And Male Infertility
Deafness, Sensorineural, And Male Infertility 		3 0 2 0.33 0 0
CUI: C2751811
Disease: Spermatogenic Failure 7
Spermatogenic Failure 7 		4 0 2 0.29 0 0
CUI: C4023001
Disease: Nonmotile sperm
Nonmotile sperm 		6 0 2 0.22 0 0
CUI: C0393602
Disease: Isolated cervical dystonia
Isolated cervical dystonia 		1 0 1 0.20 0 0
CUI: C0730364
Disease: Idiopathic polypoidal choroidal vasculopathy
Idiopathic polypoidal choroidal vasculopathy 		1 0 1 0.20 0 0
CUI: C1843542
Disease: T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC
T-CELL PROLYMPHOCYTIC LEUKEMIA, SOMATIC 		1 0 1 0.20 0 0
CUI: C1859624
Disease: Defective B cell differentiation
Defective B cell differentiation 		1 0 1 0.20 0 0
CUI: C3825373
Disease: Hodgkin's disease in children
Hodgkin's disease in children 		1 0 1 0.20 0 0
CUI: C4020789
Disease: Abnormal sperm development
Abnormal sperm development 		1 0 1 0.20 0 0
CUI: C0342387
Disease: LH - luteinizing hormone deficiency
LH - luteinizing hormone deficiency 		2 0 1 0.17 0 0
CUI: C1858916
Disease: DEAFNESS, AUTOSOMAL DOMINANT 16
DEAFNESS, AUTOSOMAL DOMINANT 16 		2 0 1 0.17 0 0
CUI: C1876175
Disease: Ataxia-Telangiectasia Variant
Ataxia-Telangiectasia Variant 		2 0 1 0.17 0 0
CUI: C4017102
Disease: ATAXIA-TELANGIECTASIA WITHOUT IMMUNODEFICIENCY
ATAXIA-TELANGIECTASIA WITHOUT IMMUNODEFICIENCY 		2 0 1 0.17 0 0
CUI: C0263606
Disease: Early radiation dermatitis
Early radiation dermatitis 		3 0 1 0.14 0 0
CUI: C0406587
Disease: Wrinkly skin syndrome
Wrinkly skin syndrome 		3 0 1 0.14 0 0
CUI: C1863561
Disease: Deafness, Autosomal Recessive 16
Deafness, Autosomal Recessive 16 		3 0 1 0.14 0 0
CUI: C1968706
Disease: Hypoplasia of the fallopian tube
Hypoplasia of the fallopian tube 		3 0 1 0.14 0 0
CUI: C3249875
Disease: Laryngopharyngeal Cancer
Laryngopharyngeal Cancer 		3 0 1 0.14 0 0
CUI: C3547187
Disease: response to metformin
response to metformin 		3 0 1 0.14 0 0
CUI: C4551901
Disease: OTOSCLEROSIS 1
OTOSCLEROSIS 1 		3 0 1 0.14 0 0
CUI: C4023703
Disease: Abnormality of the Leydig cells
Abnormality of the Leydig cells 		4 0 1 0.12 0 0
CUI: C4024276
Disease: Peripheral Schwannoma
Peripheral Schwannoma 		4 0 1 0.12 0 0
CUI: C0220702
Disease: SCHIZOPHRENIA 1 (disorder)
SCHIZOPHRENIA 1 (disorder) 		5 0 1 0.11 0 0
CUI: C0555202
Disease: Malignant lymphoma - lymphocytic, intermediate differentiation
Malignant lymphoma - lymphocytic, intermediate differentiation 		5 0 1 0.11 0 0
CUI: C1832828
Disease: Deafness, Autosomal Recessive 9
Deafness, Autosomal Recessive 9 		5 0 1 0.11 0 0