Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Hypocalciuric Hypercalcemia, Acquired
13 0 11 0.13 0 0
CUI: C0034012
Disease: Delayed Puberty
Delayed Puberty
196 21 32 0.13 8 0.10
CUI: C1535964
Disease: Cholestatic pruritus
Cholestatic pruritus
15 0 11 0.13 0 0
POLYMICROGYRIA, BILATERAL FRONTOPARIETAL
15 0 11 0.13 0 0
CUI: C0580174
Disease: Portal hypertensive gastropathy
Portal hypertensive gastropathy
24 0 12 0.13 0 0
CUI: C0022735
Disease: Klinefelter Syndrome
Klinefelter Syndrome
150 18 26 0.13 4 5.0E-02
CUI: C4552011
Disease: Gonadotropin deficiency
Gonadotropin deficiency
26 0 12 0.12 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis
217 0 33 0.12 0 0
CUI: C0342443
Disease: Adrenal Cushing's syndrome
Adrenal Cushing's syndrome
120 0 22 0.12 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect
94 0 19 0.12 0 0
Congenital absence of kidneys syndrome
110 0 20 0.12 0 0
CUI: C1827524
Disease: Wide spaced nipples
Wide spaced nipples
96 0 18 0.11 0 0
CUI: C0087169
Disease: Withdrawal Symptoms
Withdrawal Symptoms
126 0 21 0.11 0 0
CUI: C0018834
Disease: Heartburn
Heartburn
139 0 22 0.11 0 0
CUI: C0241893
Disease: Tick fever
Tick fever
9 0 9 0.11 0 0
CUI: C0276849
Disease: Infection by Babesia bovis
Infection by Babesia bovis
9 0 9 0.11 0 0
CUI: C1274989
Disease: Retinoid dermatitis
Retinoid dermatitis
9 0 9 0.11 0 0
CUI: C0936282
Disease: Blastoma
Blastoma
20 0 10 0.11 0 0
CUI: C0157743
Disease: Vibratory urticaria
Vibratory urticaria
10 0 9 0.11 0 0
CUI: C3805574
Disease: Increased fracture rate
Increased fracture rate
123 0 20 0.11 0 0
CUI: C0597854
Disease: renin induced hypertension
renin induced hypertension
11 0 9 0.11 0 0
Primary pigmented nodular adrenocortical disease
22 0 10 0.11 0 0
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8
13 0 9 0.10 0 0
Nephrogenic Syndrome of Inappropriate Antidiuresis
14 0 9 0.10 0 0
CUI: C0032002
Disease: Pituitary Diseases
Pituitary Diseases
153 0 22 0.10 0 0