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: C1960539
Disease: Aromatase deficiency
Aromatase deficiency 		6 0 2 0.22 0 0
CUI: C0016697
Disease: Freemartinism
Freemartinism 		1 0 1 0.20 0 0
CUI: C0241616
Disease: Atrophy of vagina
Atrophy of vagina 		1 0 1 0.20 0 0
CUI: C0268285
Disease: Adrenal hyperplasia, congenital, type 5
Adrenal hyperplasia, congenital, type 5 		7 0 2 0.20 0 0
CUI: C0271629
Disease: Mullerian inhibiting factor deficiency
Mullerian inhibiting factor deficiency 		1 0 1 0.20 0 0
CUI: C0342544
Disease: Idiopathic central precocious puberty
Idiopathic central precocious puberty 		13 0 3 0.20 0 0
CUI: C0342548
Disease: Early menarche
Early menarche 		1 0 1 0.20 0 0
CUI: C0404562
Disease: Incipient ovarian failure
Incipient ovarian failure 		1 0 1 0.20 0 0
CUI: C0432273
Disease: Worth disease
Worth disease 		1 0 1 0.20 0 0
CUI: C0521516
Disease: Polymyalgia
Polymyalgia 		1 0 1 0.20 0 0
CUI: C1563718
Disease: Genital Infantilism
Genital Infantilism 		1 0 1 0.20 0 0
CUI: C1840419
Disease: Metacarpal diaphyseal endosteal sclerosis
Metacarpal diaphyseal endosteal sclerosis 		1 0 1 0.20 0 0
CUI: C1840420
Disease: Metatarsal diaphyseal endosteal sclerosis
Metatarsal diaphyseal endosteal sclerosis 		1 0 1 0.20 0 0
CUI: C1842154
Disease: Sclerotic vertebral body
Sclerotic vertebral body 		1 0 1 0.20 0 0
CUI: C1843323
Disease: Van Buchem disease type 2
Van Buchem disease type 2 		1 0 1 0.20 0 0
CUI: C1843330
Disease: OSTEOPETROSIS, AUTOSOMAL DOMINANT 1
OSTEOPETROSIS, AUTOSOMAL DOMINANT 1 		1 0 1 0.20 0 0
CUI: C1866079
Disease: BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1
BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 1 		1 0 1 0.20 0 0
CUI: C1866080
Disease: HIGH BONE MASS
HIGH BONE MASS 		1 0 1 0.20 0 0
CUI: C1866176
Disease: EXUDATIVE VITREORETINOPATHY 4 (disorder)
EXUDATIVE VITREORETINOPATHY 4 (disorder) 		1 0 1 0.20 0 0
CUI: C1960540
Disease: Placental aromatase deficiency
Placental aromatase deficiency 		1 0 1 0.20 0 0
CUI: C3160829
Disease: Urogenital atrophy
Urogenital atrophy 		1 0 1 0.20 0 0
CUI: C3161177
Disease: Autoimmune hemophilia
Autoimmune hemophilia 		1 0 1 0.20 0 0
CUI: C3281153
Disease: EFAVIRENZ, POOR METABOLISM OF
EFAVIRENZ, POOR METABOLISM OF 		1 0 1 0.20 0 0
CUI: C3553841
Disease: HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA
HYPOGONADOTROPIC HYPOGONADISM 8 WITH OR WITHOUT ANOSMIA 		1 0 1 0.20 0 0
CUI: C3554669
Disease: Clavicular sclerosis
Clavicular sclerosis 		1 0 1 0.20 0 0