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: C0425957
Disease: Secondary amenorrhea
Secondary amenorrhea
49 0 14 0.24 0 0
Congenital hypogonadotropic hypogonadism
23 0 9 0.24 0 0
CUI: C1563720
Disease: Kallmann Syndrome 2 (disorder)
Kallmann Syndrome 2 (disorder)
8 0 6 0.23 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect
94 0 22 0.23 0 0
CUI: C0232940
Disease: Secondary physiologic amenorrhea
Secondary physiologic amenorrhea
58 0 15 0.22 0 0
Idiopathic hypogonadotropic hypogonadism
82 0 19 0.22 0 0
CUI: C0220748
Disease: Cartilage-hair hypoplasia
Cartilage-hair hypoplasia
49 0 13 0.22 0 0
CUI: C1862863
Disease: Sparse body hair
Sparse body hair
57 0 14 0.21 0 0
CUI: C1563719
Disease: Kallmann Syndrome 1
Kallmann Syndrome 1
12 0 6 0.20 0 0
Congenital absence of kidneys syndrome
110 0 22 0.20 0 0
CUI: C0018418
Disease: Gynecomastia
Gynecomastia
121 0 23 0.19 0 0
Congenital sensorineural hearing loss
68 0 14 0.18 0 0
CUI: C1858573
Disease: Sparse pubic hair
Sparse pubic hair
42 0 10 0.18 0 0
CUI: C0232939
Disease: Primary physiologic amenorrhea
Primary physiologic amenorrhea
129 0 23 0.18 0 0
Constitutional delay of growth and puberty
16 0 6 0.18 0 0
CUI: C3805574
Disease: Increased fracture rate
Increased fracture rate
123 0 22 0.18 0 0
CUI: C0241355
Disease: Small testicle
Small testicle
129 0 22 0.17 0 0
CUI: C1858574
Disease: Sparse axillary hair
Sparse axillary hair
39 0 9 0.17 0 0
Gonadotropin releasing factor deficiency
5 0 4 0.16 0 0
CUI: C0338503
Disease: Septo-Optic Dysplasia
Septo-Optic Dysplasia
35 0 8 0.16 0 0
Hypogonadism, Isolated Hypogonadotropic
42 0 8 0.14 0 0
CUI: C1827524
Disease: Wide spaced nipples
Wide spaced nipples
96 0 14 0.13 0 0
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism
178 0 23 0.13 0 0
CUI: C4551492
Disease: Micropenis
Micropenis
32 0 6 0.12 0 0
CUI: C0410528
Disease: Skeletal dysplasia
Skeletal dysplasia
186 0 22 0.12 0 0