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: C4025821
Disease: Anterior hypopituitarism
Anterior hypopituitarism 		48 0 13 0.15 0 0
CUI: C1862863
Disease: Sparse body hair
Sparse body hair 		57 0 14 0.15 0 0
CUI: C0520927
Disease: Decreased fertility
Decreased fertility 		50 0 13 0.15 0 0
CUI: C0342384
Disease: Idiopathic hypogonadotropic hypogonadism
Idiopathic hypogonadotropic hypogonadism 		82 0 17 0.15 0 0
CUI: C3489396
Disease: Hypogonadism, Isolated Hypogonadotropic
Hypogonadism, Isolated Hypogonadotropic 		42 0 11 0.14 0 0
CUI: C0030486
Disease: Paraplegia
Paraplegia 		59 0 13 0.14 0 0
CUI: C4552011
Disease: Gonadotropin deficiency
Gonadotropin deficiency 		26 0 9 0.14 0 0
CUI: C1865866
Disease: Congenital sensorineural hearing loss
Congenital sensorineural hearing loss 		68 0 14 0.14 0 0
CUI: C4024202
Disease: Reduced number of teeth
Reduced number of teeth 		67 0 13 0.13 0 0
CUI: C1563720
Disease: Kallmann Syndrome 2 (disorder)
Kallmann Syndrome 2 (disorder) 		8 45 6 0.12 1 8.3E-03
CUI: C2674432
Disease: Reduced bone mineral density
Reduced bone mineral density 		76 0 13 0.12 0 0
CUI: C0232939
Disease: Primary physiologic amenorrhea
Primary physiologic amenorrhea 		129 0 18 0.11 0 0
CUI: C1858573
Disease: Sparse pubic hair
Sparse pubic hair 		42 0 9 0.11 0 0
CUI: C1563719
Disease: Kallmann Syndrome 1
Kallmann Syndrome 1 		12 0 6 0.11 0 0
CUI: C1827524
Disease: Wide spaced nipples
Wide spaced nipples 		96 0 14 0.11 0 0
CUI: C0241355
Disease: Small testicle
Small testicle 		129 0 17 0.11 0 0
CUI: C1328577
Disease: Empty follicle syndrome
Empty follicle syndrome 		14 0 6 0.11 0 0
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		178 0 21 0.10 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 13 1.0E-01 0 0
CUI: C0342138
Disease: Thyrotoxicosis in pregnancy
Thyrotoxicosis in pregnancy 		6 0 5 1.0E-01 0 0
CUI: C1858574
Disease: Sparse axillary hair
Sparse axillary hair 		39 0 8 1.0E-01 0 0
CUI: C2930927
Disease: Kallmann syndrome, type 3, recessive
Kallmann syndrome, type 3, recessive 		6 0 5 1.0E-01 0 0
CUI: C0334524
Disease: Mixed Germ Cell Tumor
Mixed Germ Cell Tumor 		8 0 5 9.6E-02 0 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition 		140 0 16 9.2E-02 0 0
CUI: C0338503
Disease: Septo-Optic Dysplasia
Septo-Optic Dysplasia 		35 0 7 9.1E-02 0 0