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: C4552079
Disease: Premature Ovarian Failure 1
Premature Ovarian Failure 1 		7 0 6 0.86 0 0
CUI: C0086367
Disease: Gonadotropin-Resistant Ovary Syndrome
Gonadotropin-Resistant Ovary Syndrome 		9 0 6 0.67 0 0
CUI: C0949331
Disease: Gonadal Agenesis
Gonadal Agenesis 		2 0 2 0.33 0 0
CUI: C0007166
Disease: Low Cardiac Output
Low Cardiac Output 		1 0 1 0.17 0 0
CUI: C0341117
Disease: Esophageal erosions
Esophageal erosions 		1 0 1 0.17 0 0
CUI: C0432482
Disease: Fragile X chromosome
Fragile X chromosome 		1 0 1 0.17 0 0
CUI: C0600177
Disease: Low Cardiac Output Syndrome
Low Cardiac Output Syndrome 		1 0 1 0.17 0 0
CUI: C0679378
Disease: neurodevelopmental anomaly
neurodevelopmental anomaly 		1 0 1 0.17 0 0
CUI: C0851121
Disease: digestive problem
digestive problem 		1 0 1 0.17 0 0
CUI: C1319016
Disease: Nephrogenic rest, intralobar
Nephrogenic rest, intralobar 		1 0 1 0.17 0 0
CUI: C1536114
Disease: Central pain syndrome
Central pain syndrome 		1 0 1 0.17 0 0
CUI: C1836023
Disease: Drug Metabolism, Poor, CYP2C19-Related
Drug Metabolism, Poor, CYP2C19-Related 		1 0 1 0.17 0 0
CUI: C1837026
Disease: MEACHAM SYNDROME (disorder)
MEACHAM SYNDROME (disorder) 		1 0 1 0.17 0 0
CUI: C1839785
Disease: Folate-dependent fragile site at Xq28
Folate-dependent fragile site at Xq28 		1 0 1 0.17 0 0
CUI: C1860268
Disease: Gonadal tissue inappropriate for external genitalia or chromosomal sex
Gonadal tissue inappropriate for external genitalia or chromosomal sex 		1 0 1 0.17 0 0
CUI: C2751825
Disease: PREMATURE OVARIAN FAILURE 7 (disorder)
PREMATURE OVARIAN FAILURE 7 (disorder) 		1 0 1 0.17 0 0
CUI: C3151406
Disease: SPERMATOGENIC FAILURE 8
SPERMATOGENIC FAILURE 8 		1 0 1 0.17 0 0
CUI: C3151568
Disease: NEPHROTIC SYNDROME, TYPE 4
NEPHROTIC SYNDROME, TYPE 4 		1 0 1 0.17 0 0
CUI: C3264595
Disease: Agoraphobia without panic disorder
Agoraphobia without panic disorder 		1 0 1 0.17 0 0
CUI: C3275367
Disease: Impaired tandem gait
Impaired tandem gait 		1 0 1 0.17 0 0
CUI: C3275521
Disease: CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME
CHROMOSOME Xq27.3-q28 DUPLICATION SYNDROME 		1 0 1 0.17 0 0
CUI: C3805515
Disease: Microorchidism
Microorchidism 		1 0 1 0.17 0 0
CUI: C3806711
Disease: ANGIOEDEMA INDUCED BY ACE INHIBITORS, SUSCEPTIBILITY TO
ANGIOEDEMA INDUCED BY ACE INHIBITORS, SUSCEPTIBILITY TO 		1 0 1 0.17 0 0
CUI: C4024650
Disease: Congenital macroorchidism
Congenital macroorchidism 		1 0 1 0.17 0 0
CUI: C4479664
Disease: ADRENAL INSUFFICIENCY, NR5A1-RELATED
ADRENAL INSUFFICIENCY, NR5A1-RELATED 		1 0 1 0.17 0 0