Source: CURATED ×
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: C1257877
Disease: Pheochromocytoma, Extra-Adrenal
Pheochromocytoma, Extra-Adrenal 		16 0 16 0.84 0 0
CUI: C1708353
Disease: Hereditary Paraganglioma-Pheochromocytoma Syndrome
Hereditary Paraganglioma-Pheochromocytoma Syndrome 		23 98 11 0.35 41 0.20
CUI: C1847319
Disease: PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA
PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA 		6 33 6 0.32 32 0.21
CUI: C1704374
Disease: Carcinoma of Endocrine Gland
Carcinoma of Endocrine Gland 		15 0 8 0.31 0 0
CUI: C0206695
Disease: Carcinoma, Neuroendocrine
Carcinoma, Neuroendocrine 		12 0 7 0.29 0 0
CUI: C0030421
Disease: Paraganglioma
Paraganglioma 		13 10 7 0.28 6 3.9E-02
CUI: C0349535
Disease: Carcinoid tumor of intestine
Carcinoid tumor of intestine 		4 0 4 0.21 0 0
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple 		9 107 3 0.12 1 3.9E-03
CUI: C0004930
Disease: Behavior Disorders
Behavior Disorders 		12 0 3 0.11 0 0
CUI: C0004936
Disease: Mental disorders
Mental disorders 		12 0 3 0.11 0 0
CUI: C0376338
Disease: Diagnosis, Psychiatric
Diagnosis, Psychiatric 		12 0 3 0.11 0 0
CUI: C0393574
Disease: Huntington Disease, Late Onset
Huntington Disease, Late Onset 		12 0 3 0.11 0 0
CUI: C0751207
Disease: Akinetic-Rigid Variant of Huntington Disease
Akinetic-Rigid Variant of Huntington Disease 		12 0 3 0.11 0 0
CUI: C0751208
Disease: Juvenile Huntington Disease
Juvenile Huntington Disease 		12 0 3 0.11 0 0
CUI: C4046029
Disease: Mental Disorders, Severe
Mental Disorders, Severe 		12 0 3 0.11 0 0
CUI: C1861848
Disease: PARAGANGLIOMAS 4
PARAGANGLIOMAS 4 		2 67 2 0.11 57 0.36
CUI: C1306067
Disease: Drug-induced paranoid state
Drug-induced paranoid state 		3 0 2 1.0E-01 0 0
CUI: C1855008
Disease: Mitochondrial Complex II Deficiency
Mitochondrial Complex II Deficiency 		4 44 2 9.5E-02 1 5.2E-03
CUI: C0020179
Disease: Huntington Disease
Huntington Disease 		17 0 3 9.1E-02 0 0
CUI: C1859049
Disease: CCHS WITH HIRSCHSPRUNG DISEASE
CCHS WITH HIRSCHSPRUNG DISEASE 		5 0 2 9.1E-02 0 0
CUI: C3888239
Disease: HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 		6 52 2 8.7E-02 4 2.0E-02
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		7 13 2 8.3E-02 4 2.5E-02
CUI: C0032461
Disease: Polycythemia
Polycythemia 		8 0 2 8.0E-02 0 0
CUI: C0242423
Disease: Ramsay Hunt Paralysis Syndrome
Ramsay Hunt Paralysis Syndrome 		28 0 3 6.8E-02 0 0
CUI: C0752097
Disease: Autosomal Dominant Juvenile Parkinson Disease
Autosomal Dominant Juvenile Parkinson Disease 		28 0 3 6.8E-02 0 0