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: C0751156
Disease: FRAXA Syndrome
FRAXA Syndrome 		8 0 5 0.36 0 0
CUI: C1864172
Disease: Peroxisome Biogenesis Disorder, Complementation Group G
Peroxisome Biogenesis Disorder, Complementation Group G 		10 0 3 0.17 0 0
CUI: C2673497
Disease: Leydig Cell Hypoplasia, Type II
Leydig Cell Hypoplasia, Type II 		3 0 2 0.17 0 0
CUI: C2674612
Disease: Leydig Cell Adenoma, Somatic, with Male-Limited Precocious Puberty
Leydig Cell Adenoma, Somatic, with Male-Limited Precocious Puberty 		3 0 2 0.17 0 0
CUI: C2930861
Disease: Premature ovarian failure, familial
Premature ovarian failure, familial 		3 0 2 0.17 0 0
CUI: C3668935
Disease: Luteinizing Hormone Resistance, Female
Luteinizing Hormone Resistance, Female 		3 0 2 0.17 0 0
CUI: C3825158
Disease: Learning disabled
Learning disabled 		3 0 2 0.17 0 0
CUI: C4016252
Disease: LEYDIG HYPOPLASIA, TYPE I
LEYDIG HYPOPLASIA, TYPE I 		3 0 2 0.17 0 0
CUI: C4023702
Disease: Hyoplasia of the Leydig cells
Hyoplasia of the Leydig cells 		3 0 2 0.17 0 0
CUI: C0743101
Disease: developmentally delayed
developmentally delayed 		11 0 3 0.16 0 0
CUI: C0004444
Disease: Avoidant Personality Disorder
Avoidant Personality Disorder 		4 0 2 0.15 0 0
CUI: C1859979
Disease: Precocious puberty in males
Precocious puberty in males 		5 0 2 0.14 0 0
CUI: C0266432
Disease: Leydig cell agenesis
Leydig cell agenesis 		6 0 2 0.13 0 0
CUI: C0278061
Disease: Abnormal mental state
Abnormal mental state 		24 0 3 9.4E-02 0 0
CUI: C0006542
Disease: Byssinosis
Byssinosis 		1 0 1 9.1E-02 0 0
CUI: C0030328
Disease: Panniculitis, Nodular Nonsuppurative
Panniculitis, Nodular Nonsuppurative 		1 0 1 9.1E-02 0 0
CUI: C0233585
Disease: Foot tapping
Foot tapping 		1 0 1 9.1E-02 0 0
CUI: C0241876
Disease: Obstructive emphysema
Obstructive emphysema 		1 0 1 9.1E-02 0 0
CUI: C0342610
Disease: Hereditary cerebrovascular amyloidosis
Hereditary cerebrovascular amyloidosis 		1 0 1 9.1E-02 0 0
CUI: C0343972
Disease: Schistosomal splenomegaly
Schistosomal splenomegaly 		1 0 1 9.1E-02 0 0
CUI: C0432482
Disease: Fragile X chromosome
Fragile X chromosome 		1 0 1 9.1E-02 0 0
CUI: C0679378
Disease: neurodevelopmental anomaly
neurodevelopmental anomaly 		1 0 1 9.1E-02 0 0
CUI: C0679441
Disease: Disorder of olfactory system
Disorder of olfactory system 		1 0 1 9.1E-02 0 0
CUI: C0742115
Disease: Cerebritis
Cerebritis 		1 0 1 9.1E-02 0 0
CUI: C0743188
Disease: diarrhea persistent
diarrhea persistent 		1 0 1 9.1E-02 0 0