Source: ALL
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: C0342482
Disease: X-linked Adrenal Hypoplasia
X-linked Adrenal Hypoplasia 		57 70 45 0.79 13 0.19
CUI: C0338488
Disease: Alternating hemiplegia of childhood
Alternating hemiplegia of childhood 		8 4 5 0.10 4 0.31
CUI: C0400914
Disease: Acute hepatitis C
Acute hepatitis C 		8 2 5 0.10 2 0.15
CUI: C1836623
Disease: Decreased circulating cortisol level
Decreased circulating cortisol level 		23 0 6 9.7E-02 0 0
CUI: C0405580
Disease: Adrenal cortical hypofunction
Adrenal cortical hypofunction 		52 0 8 9.0E-02 0 0
CUI: C0857899
Disease: Decreased circulating aldosterone level
Decreased circulating aldosterone level 		16 0 5 8.9E-02 0 0
CUI: C0877056
Disease: Hypoglycemic seizures
Hypoglycemic seizures 		19 0 5 8.5E-02 0 0
CUI: C0022735
Disease: Klinefelter Syndrome
Klinefelter Syndrome 		150 0 15 8.3E-02 0 0
CUI: C4284088
Disease: MIRAGE SYNDROME
MIRAGE SYNDROME 		8 0 4 8.2E-02 0 0
CUI: C4476786
Disease: Testicular adrenal rest tumor
Testicular adrenal rest tumor 		8 0 4 8.2E-02 0 0
CUI: C4696948
Disease: Trauma symptoms
Trauma symptoms 		8 0 4 8.2E-02 0 0
CUI: C1846347
Disease: Renal salt wasting
Renal salt wasting 		22 0 5 8.1E-02 0 0
CUI: C1720189
Disease: Episodic Ataxia
Episodic Ataxia 		36 0 6 8.0E-02 0 0
CUI: C0270862
Disease: Hemiplegic migraine
Hemiplegic migraine 		10 14 4 7.8E-02 2 8.0E-02
CUI: C4552011
Disease: Gonadotropin deficiency
Gonadotropin deficiency 		26 0 5 7.6E-02 0 0
CUI: C4049650
Disease: Familial Glucocorticoid Deficiency Type 1
Familial Glucocorticoid Deficiency Type 1 		12 0 4 7.5E-02 0 0
CUI: C3887896
Disease: Primary Adrenal Insufficiency
Primary Adrenal Insufficiency 		27 0 5 7.5E-02 0 0
CUI: C0162809
Disease: Kallmann Syndrome
Kallmann Syndrome 		86 0 9 7.4E-02 0 0
CUI: C1848296
Disease: DOSAGE-SENSITIVE SEX REVERSAL
DOSAGE-SENSITIVE SEX REVERSAL 		159 0 14 7.4E-02 0 0
CUI: C0001627
Disease: Congenital adrenal hyperplasia
Congenital adrenal hyperplasia 		87 0 9 7.3E-02 0 0
CUI: C4021551
Disease: Absence of secondary sex characteristics
Absence of secondary sex characteristics 		44 0 6 7.2E-02 0 0
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction 		90 0 9 7.1E-02 0 0
CUI: C0206635
Disease: Myelolipoma
Myelolipoma 		16 0 4 7.0E-02 0 0
CUI: C0020461
Disease: Hyperkalemia
Hyperkalemia 		32 0 5 6.9E-02 0 0
CUI: C0037899
Disease: Sphingolipidoses
Sphingolipidoses 		17 0 4 6.9E-02 0 0