RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0025269
Disease: Multiple Endocrine Neoplasia Type 2b
Multiple Endocrine Neoplasia Type 2b 		1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C0025269
Disease: Multiple Endocrine Neoplasia Type 2b
Multiple Endocrine Neoplasia Type 2b 		1.000 Biomarker disease CTD_human
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		1.000 CausalMutation disease CLINVAR
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		1.000 CausalMutation disease CGI
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		1.000 Biomarker disease HPO
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		1.000 Biomarker disease GENOMICS_ENGLAND
CUI: C0031511
Disease: Pheochromocytoma
Pheochromocytoma 		1.000 GeneticVariation disease CLINVAR
CUI: C0025268
Disease: Multiple Endocrine Neoplasia Type 2a
Multiple Endocrine Neoplasia Type 2a 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		0.800 GeneticVariation disease UNIPROT
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		0.800 CausalMutation disease CGI
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		0.800 GeneticVariation disease CLINVAR
CUI: C1833921
Disease: Familial medullary thyroid carcinoma
Familial medullary thyroid carcinoma 		0.800 Biomarker disease GENOMICS_ENGLAND
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		0.750 Biomarker disease GENOMICS_ENGLAND
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		0.750 CausalMutation disease CLINVAR
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		0.750 Biomarker disease GENOMICS_ENGLAND
CUI: C1275808
Disease: Congenital central hypoventilation
Congenital central hypoventilation 		0.750 GeneticVariation disease CLINVAR
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		0.740 Biomarker disease GENOMICS_ENGLAND
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		0.740 Biomarker disease HPO
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.700 Biomarker disease HPO
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.700 SusceptibilityMutation disease CLINVAR
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		0.700 GeneticVariation disease CLINVAR
CUI: C0027662
Disease: Multiple Endocrine Neoplasia
Multiple Endocrine Neoplasia 		0.700 CausalMutation disease CLINVAR
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm 		0.700 Biomarker disease HPO
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm 		0.700 CausalMutation disease CGI