Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		0.800 Biomarker disease CTD_human
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		0.800 Biomarker disease HPO
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		0.800 CausalMutation disease CGI
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
Gastrointestinal Stromal Tumors 		0.800 Biomarker group HPO
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
Gastrointestinal Stromal Tumors 		0.800 Biomarker group CTD_human
CUI: C0238198
Disease: Gastrointestinal Stromal Tumors
Gastrointestinal Stromal Tumors 		0.800 Biomarker group GENOMICS_ENGLAND
CUI: C1847319
Disease: PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA
PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA 		0.760 Biomarker disease CTD_human
CUI: C1847319
Disease: PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA
PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA 		0.760 CausalMutation disease CLINVAR
CUI: C1847319
Disease: PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA
PARAGANGLIOMA AND GASTRIC STROMAL SARCOMA 		0.760 Biomarker disease GENOMICS_ENGLAND
CUI: C1861848
Disease: PARAGANGLIOMAS 4
PARAGANGLIOMAS 4 		0.710 Biomarker disease GENOMICS_ENGLAND
CUI: C1861848
Disease: PARAGANGLIOMAS 4
PARAGANGLIOMAS 4 		0.710 Biomarker disease CTD_human
CUI: C0030421
Disease: Paraganglioma
Paraganglioma 		0.700 CausalMutation disease CGI
CUI: C0030421
Disease: Paraganglioma
Paraganglioma 		0.700 GeneticVariation disease CLINVAR
CUI: C0030421
Disease: Paraganglioma
Paraganglioma 		0.700 Biomarker disease HPO
CUI: C3179349
Disease: Gastrointestinal Stromal Sarcoma
Gastrointestinal Stromal Sarcoma 		0.500 Biomarker disease CTD_human
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple 		0.450 CausalMutation disease CLINVAR
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple 		0.450 GeneticVariation disease CLINVAR
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple 		0.450 GermlineCausalMutation disease ORPHANET
CUI: C1257877
Disease: Pheochromocytoma, Extra-Adrenal
Pheochromocytoma, Extra-Adrenal 		0.450 Biomarker disease CTD_human
CUI: C1257877
Disease: Pheochromocytoma, Extra-Adrenal
Pheochromocytoma, Extra-Adrenal 		0.450 Biomarker disease HPO
CUI: C1333993
Disease: hereditary paraganglioma
hereditary paraganglioma 		0.400 Biomarker disease GENOMICS_ENGLAND
CUI: C0740457
Disease: Malignant neoplasm of kidney
Malignant neoplasm of kidney 		0.350 Biomarker disease GENOMICS_ENGLAND
CUI: C0206695
Disease: Carcinoma, Neuroendocrine
Carcinoma, Neuroendocrine 		0.300 Biomarker disease GENOMICS_ENGLAND
CUI: C1704374
Disease: Carcinoma of Endocrine Gland
Carcinoma of Endocrine Gland 		0.300 Biomarker disease GENOMICS_ENGLAND