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: C0242343
Disease: Panhypopituitarism
Panhypopituitarism 		73 0 24 0.18 0 0
CUI: C3899503
Disease: Congenital hypogonadotropic hypogonadism
Congenital hypogonadotropic hypogonadism 		23 0 16 0.17 0 0
CUI: C0685840
Disease: Congenital hypoplasia of ovary
Congenital hypoplasia of ovary 		44 0 19 0.17 0 0
CUI: C0022735
Disease: Klinefelter Syndrome
Klinefelter Syndrome 		150 18 34 0.17 2 4.3E-02
CUI: C4024202
Disease: Reduced number of teeth
Reduced number of teeth 		67 0 22 0.17 0 0
CUI: C4552011
Disease: Gonadotropin deficiency
Gonadotropin deficiency 		26 0 16 0.17 0 0
CUI: C0220748
Disease: Cartilage-hair hypoplasia
Cartilage-hair hypoplasia 		49 0 19 0.16 0 0
CUI: C0266399
Disease: Infantile uterus
Infantile uterus 		43 0 18 0.16 0 0
CUI: C2674432
Disease: Reduced bone mineral density
Reduced bone mineral density 		76 0 22 0.16 0 0
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism 		69 4 21 0.16 1 3.0E-02
CUI: C0425957
Disease: Secondary amenorrhea
Secondary amenorrhea 		49 0 18 0.15 0 0
CUI: C0232940
Disease: Secondary physiologic amenorrhea
Secondary physiologic amenorrhea 		58 0 19 0.15 0 0
CUI: C1836308
Disease: Generalized joint laxity
Generalized joint laxity 		44 0 17 0.15 0 0
CUI: C0034012
Disease: Delayed Puberty
Delayed Puberty 		196 21 36 0.15 1 2.0E-02
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		110 0 25 0.15 0 0
CUI: C0338503
Disease: Septo-Optic Dysplasia
Septo-Optic Dysplasia 		35 19 15 0.14 1 2.1E-02
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 22 0.14 0 0
CUI: C1862863
Disease: Sparse body hair
Sparse body hair 		57 0 17 0.13 0 0
CUI: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism 		41 0 15 0.13 0 0
CUI: C1858573
Disease: Sparse pubic hair
Sparse pubic hair 		42 0 15 0.13 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis 		217 0 34 0.13 0 0
CUI: C1858574
Disease: Sparse axillary hair
Sparse axillary hair 		39 0 14 0.13 0 0
CUI: C1865866
Disease: Congenital sensorineural hearing loss
Congenital sensorineural hearing loss 		68 0 17 0.12 0 0
CUI: C3805574
Disease: Increased fracture rate
Increased fracture rate 		123 0 23 0.12 0 0
CUI: C0032002
Disease: Pituitary Diseases
Pituitary Diseases 		153 0 26 0.12 0 0