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: C0342543
Disease: Central Precocious Puberty
Central Precocious Puberty
32 0 18 0.23 0 0
Idiopathic central precocious puberty
13 0 10 0.15 0 0
CUI: C0016510
Disease: Foot Diseases
Foot Diseases
8 0 7 0.11 0 0
CUI: C0032002
Disease: Pituitary Diseases
Pituitary Diseases
153 0 19 9.6E-02 0 0
CUI: C0741682
Disease: Premenopausal breast cancer
Premenopausal breast cancer
51 18 10 9.5E-02 1 2.9E-02
Hypogonadism, Isolated Hypogonadotropic
42 0 9 9.3E-02 0 0
Immune reconstitution inflammatory syndrome [IRIS]
33 0 8 9.0E-02 0 0
CUI: C0004903
Disease: Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome
107 0 14 8.9E-02 0 0
CUI: C0034013
Disease: Precocious Puberty
Precocious Puberty
139 0 16 8.6E-02 0 0
CUI: C0405581
Disease: Testicular dysfunction
Testicular dysfunction
13 0 6 8.5E-02 0 0
CUI: C0013338
Disease: Pituitary dwarfism
Pituitary dwarfism
41 0 8 8.2E-02 0 0
CUI: C0020635
Disease: Hypopituitarism
Hypopituitarism
69 0 10 8.1E-02 0 0
CUI: C3839507
Disease: Diminished ovarian reserve
Diminished ovarian reserve
43 0 8 8.1E-02 0 0
CUI: C0342541
Disease: Precocious pubarche
Precocious pubarche
30 0 7 8.0E-02 0 0
Gastro-esophageal reflux disease with esophagitis
71 0 10 8.0E-02 0 0
CUI: C0016034
Disease: Breast Fibrocystic Disease
Breast Fibrocystic Disease
114 0 13 7.9E-02 0 0
CUI: C0020505
Disease: Hyperphagia
Hyperphagia
60 0 9 7.8E-02 0 0
CUI: C0018206
Disease: granulosa cell tumor
granulosa cell tumor
88 0 11 7.8E-02 0 0
CUI: C3665349
Disease: Secondary hypothyroidism
Secondary hypothyroidism
47 0 8 7.8E-02 0 0
CUI: C0750887
Disease: Adrenal Cancer
Adrenal Cancer
20 0 6 7.7E-02 0 0
CUI: C0151721
Disease: Testicular hypogonadism
Testicular hypogonadism
50 0 8 7.5E-02 0 0
CUI: C0001624
Disease: Adrenal Gland Neoplasms
Adrenal Gland Neoplasms
94 0 11 7.5E-02 0 0
CUI: C0271561
Disease: Somatotropin deficiency
Somatotropin deficiency
154 0 15 7.4E-02 0 0
Subacute progressive viral hepatitis
9 0 5 7.4E-02 0 0
CUI: C3554225
Disease: LEPTIN RECEPTOR DEFICIENCY
LEPTIN RECEPTOR DEFICIENCY
9 0 5 7.4E-02 0 0