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: C2752149
Disease: 46,XY Sex Reversal 4
46,XY Sex Reversal 4 		1 0 1 1.00 0 0
CUI: C2673913
Disease: Anemia, Hypochromic Microcytic, With Iron Overload
Anemia, Hypochromic Microcytic, With Iron Overload 		4 0 1 0.25 0 0
CUI: C3826102
Disease: Iron deficiency anemia in children
Iron deficiency anemia in children 		4 0 1 0.25 0 0
CUI: C1720811
Disease: Tumor of Rete Testis
Tumor of Rete Testis 		6 0 1 0.17 0 0
CUI: C1833296
Disease: FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED
FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED 		6 0 1 0.17 0 0
CUI: C4288538
Disease: Ovotesticular Differences of Sex Development
Ovotesticular Differences of Sex Development 		6 0 1 0.17 0 0
CUI: C2748895
Disease: Ovotesticular Disorders of Sex Development
Ovotesticular Disorders of Sex Development 		7 0 1 0.14 0 0
CUI: C0948120
Disease: Hepatic siderosis
Hepatic siderosis 		8 0 1 0.12 0 0
CUI: C0334517
Disease: Spermatocytic seminoma
Spermatocytic seminoma 		9 0 1 0.11 0 0
CUI: C2827503
Disease: HFE-Associated Hereditary Hemochromatosis
HFE-Associated Hereditary Hemochromatosis 		10 0 1 1.0E-01 0 0
CUI: C0302885
Disease: Testicular dysgenesis
Testicular dysgenesis 		13 0 1 7.7E-02 0 0
CUI: C0205852
Disease: Neoplasms, Embryonal and Mixed
Neoplasms, Embryonal and Mixed 		15 0 1 6.7E-02 0 0
CUI: C0751365
Disease: Cancer, Embryonal and Mixed
Cancer, Embryonal and Mixed 		15 0 1 6.7E-02 0 0
CUI: C2936694
Disease: Swyer Syndrome
Swyer Syndrome 		17 0 1 5.9E-02 0 0
CUI: C0751364
Disease: Cancer, Embryonal
Cancer, Embryonal 		18 0 1 5.6E-02 0 0
CUI: C2919755
Disease: Testicular dysgenesis syndrome
Testicular dysgenesis syndrome 		19 0 1 5.3E-02 0 0
CUI: C3550973
Disease: NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5 		19 0 1 5.3E-02 0 0
CUI: C0154208
Disease: Disorder of endocrine ovary
Disorder of endocrine ovary 		22 0 1 4.5E-02 0 0
CUI: C0271901
Disease: Microcytic hypochromic anemia (disorder)
Microcytic hypochromic anemia (disorder) 		25 0 1 4.0E-02 0 0
CUI: C0432470
Disease: 46, XY female
46, XY female 		25 0 1 4.0E-02 0 0
CUI: C0018054
Disease: Gonadal Dysgenesis, 46,XY
Gonadal Dysgenesis, 46,XY 		29 0 1 3.4E-02 0 0
CUI: C0019269
Disease: Hermaphroditism
Hermaphroditism 		34 0 1 2.9E-02 0 0
CUI: C0027658
Disease: Neoplasms, Germ Cell and Embryonal
Neoplasms, Germ Cell and Embryonal 		34 0 1 2.9E-02 0 0
CUI: C0206661
Disease: Gonadoblastoma
Gonadoblastoma 		34 0 1 2.9E-02 0 0
CUI: C0036875
Disease: Disorders of Sex Development
Disorders of Sex Development 		39 0 1 2.6E-02 0 0