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: C0342369
Disease: Somatotroph hyperplasia
Somatotroph hyperplasia
1 0 1 1.00 0 0
Specific disorders of sleep of non-organic origin
3 0 1 0.33 0 0
Isolated Growth Hormone Deficiency, Type IB
3 0 1 0.33 0 0
CUI: C4552171
Disease: Familial acromegaly
Familial acromegaly
3 0 1 0.33 0 0
ISOLATED GROWTH HORMONE DEFICIENCY, TYPE V
3 0 1 0.33 0 0
CUI: C0340987
Disease: Splenic atrophy
Splenic atrophy
4 0 1 0.25 0 0
CUI: C2932716
Disease: Pseudohypoparathyroidism Type 1C
Pseudohypoparathyroidism Type 1C
4 0 1 0.25 0 0
CUI: C1720505
Disease: Adult growth hormone deficiency
Adult growth hormone deficiency
6 0 1 0.17 0 0
CUI: C4013426
Disease: Bronchial carcinoid
Bronchial carcinoid
7 0 1 0.14 0 0
CUI: C0221405
Disease: Pituitary cachexia
Pituitary cachexia
8 0 1 0.12 0 0
CUI: C0271577
Disease: Isolated gonadotropin deficiency
Isolated gonadotropin deficiency
8 0 1 0.12 0 0
CUI: C1336746
Disease: Thymic Carcinoid Tumor
Thymic Carcinoid Tumor
8 0 1 0.12 0 0
Isolated deficiency of pituitary hormone
8 0 1 0.12 0 0
Necrosis of pituitary gland (postpartum)
8 0 1 0.12 0 0
CUI: C2874190
Disease: Pituitary short stature
Pituitary short stature
8 0 1 0.12 0 0
HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 3
8 0 1 0.12 0 0
CHROMOSOME Xq26.3 DUPLICATION SYNDROME
8 0 1 0.12 0 0
Isolated lutropin deficiency (disorder)
9 0 1 0.11 0 0
Idiopathic growth hormone deficiency
10 0 1 1.0E-01 0 0
CUI: C0268233
Disease: GALACTOSIALIDOSIS
GALACTOSIALIDOSIS
12 0 1 8.3E-02 0 0
CUI: C0268425
Disease: Alstrom Syndrome
Alstrom Syndrome
12 0 1 8.3E-02 0 0
CUI: C0751230
Disease: Hypothalamic Dysfunction Syndromes
Hypothalamic Dysfunction Syndromes
12 0 1 8.3E-02 0 0
CUI: C0855173
Disease: Placental Choriocarcinoma
Placental Choriocarcinoma
13 0 1 7.7E-02 0 0
CUI: C1864100
Disease: PSEUDOHYPOPARATHYROIDISM, TYPE IB
PSEUDOHYPOPARATHYROIDISM, TYPE IB
13 0 1 7.7E-02 0 0
CUI: C0033835
Disease: Pseudopseudohypoparathyroidism
Pseudopseudohypoparathyroidism
14 0 1 7.1E-02 0 0