RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C0749474
Disease: thyroid nodule solitary
thyroid nodule solitary
disease Neoplasms; Endocrine System Diseases Disease or Syndrome 1 0.010 None 1.000 1 1998 1998
CUI: C3544229
Disease: Congenital intestinal obstruction
Congenital intestinal obstruction
disease Congenital Abnormality 1 0.010 None 1.000 1 2018 2018
CUI: C4733537
Disease: recurrent medullary thyroid cancer
recurrent medullary thyroid cancer
disease Neoplasms; Endocrine System Diseases Neoplastic Process 1 0.010 None 1.000 1 2008 2008
CUI: C3805845
Disease: Cutaneous lichen amyloidosis
Cutaneous lichen amyloidosis
phenotype Finding 1 0.100 None 0
MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITHOUT PHEOCHROMOCYTOMA
disease Neoplastic Process 1 1 0.100 None 0 1
MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITH HIRSCHSPRUNG DISEASE
disease Neoplastic Process 1 2 0.100 None 0 2
Abnormality of enteric ganglion morphology
phenotype Anatomical Abnormality 1 0.100 None 0
CUI: C0345240
Disease: Total intestinal aganglionosis
Total intestinal aganglionosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 2 2 0.070 None 1.000 7 1997 2013
Childhood Thyroid Gland Papillary Carcinoma
disease Neoplasms; Endocrine System Diseases Neoplastic Process 2 0.030 None 1.000 3 1996 2014
CUI: C0278681
Disease: metastatic parathyroid cancer
metastatic parathyroid cancer
disease Neoplasms; Endocrine System Diseases Neoplastic Process 2 1 0.010 None 1.000 1 1 1997 1997
CUI: C0332909
Disease: Congenital unilateral absence
Congenital unilateral absence
disease Congenital Abnormality 2 0.010 None 1.000 1 2008 2008
CUI: C0345245
Disease: Hyperganglionosis
Hyperganglionosis
disease Disease or Syndrome 2 1 0.010 None 1.000 1 1 2019 2019
CUI: C3812899
Disease: Papillary carcinoma of the breast
Papillary carcinoma of the breast
disease Neoplasms Neoplastic Process 2 0.010 None < 0.001 1 2009 2009
Elevated urinary vanillylmandelic acid
phenotype Finding 2 0.100 None 0
CUI: C0878627
Disease: Mucosal neuromas
Mucosal neuromas
disease Neoplasms Disease or Syndrome 3 0.020 None 1.000 2 1998 2008
Neuronal Intestinal Dysplasia, Type B
disease Digestive System Diseases; Nervous System Diseases Disease or Syndrome 3 0.010 None 1.000 1 1996 1996
CUI: C3649644
Disease: Congenital condition
Congenital condition
disease Disease or Syndrome 3 0.010 None 1.000 1 2018 2018
CUI: C4025761
Disease: Abnormality of the integument
Abnormality of the integument
disease Anatomical Abnormality 3 1 0.100 None 0
Adenocarcinoma with neuroendocrine differentiation
disease Neoplasms Neoplastic Process 4 0.010 None 1.000 1 2017 2017
Short segment Hirschsprung's disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases Congenital Abnormality 5 1 0.030 None 1.000 3 1997 2017
Malignant neoplasm of endocrine gland
disease Neoplasms; Endocrine System Diseases Neoplastic Process 5 0.010 None 1.000 1 2018 2018
CUI: C0271633
Disease: Disorder of endocrine pancreas
Disorder of endocrine pancreas
group Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Endocrine System Diseases Disease or Syndrome 6 0.020 None 1.000 2 2017 2019
CUI: C0546275
Disease: Hypoganglionosis
Hypoganglionosis
disease Disease or Syndrome 6 1 0.020 None 1.000 2 2001 2011
CUI: C0854914
Disease: Retinoblastoma bilateral
Retinoblastoma bilateral
disease Neoplasms; Eye Diseases Neoplastic Process 6 0.010 None < 0.001 1 1995 1995
CUI: C1096168
Disease: Chromosome 17 trisomy
Chromosome 17 trisomy
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 6 0.010 None 1.000 1 2008 2008