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: C1844562
Disease: Medial flaring of the eyebrow
Medial flaring of the eyebrow
28 0 22 0.44 0 0
CUI: C4022675
Disease: Increased female libido
Increased female libido
18 0 18 0.41 0 0
CUI: C4025901
Disease: Abnormality of body height
Abnormality of body height
18 0 18 0.41 0 0
CUI: C4025569
Disease: Eunuchoid habitus
Eunuchoid habitus
21 0 18 0.38 0 0
CUI: C1846228
Disease: Absence of pubertal development
Absence of pubertal development
24 0 18 0.36 0 0
CUI: C0271578
Disease: Female hypogonadism syndrome
Female hypogonadism syndrome
25 0 18 0.35 0 0
CUI: C2936862
Disease: Bardet-Biedl syndrome 1 (disorder)
Bardet-Biedl syndrome 1 (disorder)
20 0 15 0.31 0 0
Absence of secondary sex characteristics
44 0 20 0.29 0 0
CUI: C4073137
Disease: Decreased serum testosterone level
Decreased serum testosterone level
47 0 20 0.28 0 0
CUI: C0266013
Disease: Congenital hypoplasia of breast
Congenital hypoplasia of breast
38 0 18 0.28 0 0
CUI: C0151721
Disease: Testicular hypogonadism
Testicular hypogonadism
50 0 20 0.27 0 0
Hypothalamic gonadotropin-releasing hormone deficiency
22 0 14 0.27 0 0
CUI: C0266399
Disease: Infantile uterus
Infantile uterus
43 0 18 0.26 0 0
CUI: C4022003
Disease: Erectile abnormalities
Erectile abnormalities
24 0 14 0.26 0 0
CUI: C1836308
Disease: Generalized joint laxity
Generalized joint laxity
44 0 18 0.26 0 0
CUI: C0425957
Disease: Secondary amenorrhea
Secondary amenorrhea
49 0 18 0.24 0 0
CUI: C0003126
Disease: Anosmia
Anosmia
40 0 15 0.22 0 0
CUI: C1862863
Disease: Sparse body hair
Sparse body hair
57 0 18 0.22 0 0
CUI: C0752166
Disease: Bardet-Biedl Syndrome
Bardet-Biedl Syndrome
86 0 23 0.21 0 0
CUI: C0232940
Disease: Secondary physiologic amenorrhea
Secondary physiologic amenorrhea
58 0 18 0.21 0 0
CUI: C4021776
Disease: Abnormality of the voice
Abnormality of the voice
64 0 19 0.21 0 0
CUI: C2364082
Disease: Sense of smell impaired
Sense of smell impaired
60 0 18 0.21 0 0
CUI: C1384606
Disease: Dyspareunia
Dyspareunia
37 0 14 0.21 0 0
CUI: C0454455
Disease: Mirror movements disorder
Mirror movements disorder
39 0 14 0.20 0 0
Congenital hypogonadotropic hypogonadism
23 0 11 0.20 0 0