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: C0342386
Disease: Follicle stimulating hormone deficiency
Follicle stimulating hormone deficiency 		11 0 7 0.23 0 0
CUI: C4022675
Disease: Increased female libido
Increased female libido 		18 0 8 0.22 0 0
CUI: C4025901
Disease: Abnormality of body height
Abnormality of body height 		18 0 8 0.22 0 0
CUI: C0342388
Disease: Adrenocorticotropic hormone (ACTH) deficiency (disorder)
Adrenocorticotropic hormone (ACTH) deficiency (disorder) 		24 0 9 0.22 0 0
CUI: C1846228
Disease: Absence of pubertal development
Absence of pubertal development 		24 0 9 0.22 0 0
CUI: C0271578
Disease: Female hypogonadism syndrome
Female hypogonadism syndrome 		25 0 9 0.21 0 0
CUI: C3489396
Disease: Hypogonadism, Isolated Hypogonadotropic
Hypogonadism, Isolated Hypogonadotropic 		42 0 12 0.21 0 0
CUI: C4025569
Disease: Eunuchoid habitus
Eunuchoid habitus 		21 0 8 0.21 0 0
CUI: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism 		41 0 11 0.20 0 0
CUI: C3899503
Disease: Congenital hypogonadotropic hypogonadism
Congenital hypogonadotropic hypogonadism 		23 0 8 0.20 0 0
CUI: C0151721
Disease: Testicular hypogonadism
Testicular hypogonadism 		50 0 12 0.19 0 0
CUI: C4021551
Disease: Absence of secondary sex characteristics
Absence of secondary sex characteristics 		44 0 11 0.19 0 0
CUI: C0266013
Disease: Congenital hypoplasia of breast
Congenital hypoplasia of breast 		38 0 10 0.19 0 0
CUI: C4073137
Disease: Decreased serum testosterone level
Decreased serum testosterone level 		47 0 11 0.18 0 0
CUI: C0338503
Disease: Septo-Optic Dysplasia
Septo-Optic Dysplasia 		35 0 9 0.17 0 0
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		86 0 16 0.17 0 0
CUI: C0242343
Disease: Panhypopituitarism
Panhypopituitarism 		73 0 14 0.16 0 0
CUI: C0342381
Disease: Idiopathic growth hormone deficiency
Idiopathic growth hormone deficiency 		10 0 5 0.16 0 0
CUI: C4551492
Disease: Micropenis
Micropenis 		32 0 8 0.16 0 0
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism 		69 0 13 0.16 0 0
CUI: C0266399
Disease: Infantile uterus
Infantile uterus 		43 0 9 0.15 0 0
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism 		47 0 9 0.14 0 0
CUI: C0003126
Disease: Anosmia
Anosmia 		40 0 8 0.14 0 0
CUI: C0220748
Disease: Cartilage-hair hypoplasia
Cartilage-hair hypoplasia 		49 0 9 0.14 0 0
CUI: C0242342
Disease: Sheehan Syndrome
Sheehan Syndrome 		16 0 5 0.14 0 0