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: C0041207
Disease: Truncus Arteriosus, Persistent
Truncus Arteriosus, Persistent
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 76 4 0.010 None 1.000 1 2005 2005
CUI: C0521158
Disease: Recurrent tumor
Recurrent tumor
phenotype Neoplastic Process 735 33 0.010 None < 0.001 1 1999 1999
CUI: C0035335
Disease: Retinoblastoma
Retinoblastoma
disease Neoplasms; Eye Diseases Neoplastic Process 853 193 0.010 None 1.000 1 1997 1997
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases
group Eye Diseases Disease or Syndrome 714 56 0.010 None 1.000 1 2016 2016
Acute myeloid leukemia, minimal differentiation
disease Neoplasms Neoplastic Process 33 0.010 None 1.000 1 1998 1998
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
disease Nutritional and Metabolic Diseases Disease or Syndrome 1125 591 0.010 None 1.000 1 2013 2013
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms
group Neoplasms; Male Urogenital Diseases Neoplastic Process 1722 31 0.010 None 1.000 1 2018 2018
CUI: C0033036
Disease: Atrial Premature Complexes
Atrial Premature Complexes
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 183 21 0.010 None 1.000 1 2005 2005
CUI: C0545074
Disease: Myxoid/Round Cell Liposarcoma
Myxoid/Round Cell Liposarcoma
disease Neoplasms Neoplastic Process 61 0.010 None 1.000 1 2016 2016
CUI: C0032002
Disease: Pituitary Diseases
Pituitary Diseases
group Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 153 3 0.010 None 1.000 1 2014 2014
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 83 46 0.010 None 1.000 1 2001 2001
CUI: C0553580
Disease: Ewings sarcoma
Ewings sarcoma
disease Neoplasms Neoplastic Process 517 25 0.010 None 1.000 1 2019 2019
CUI: C0553723
Disease: Squamous cell carcinoma of skin
Squamous cell carcinoma of skin
disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 458 92 0.010 None 1.000 1 2017 2017
CUI: C0030472
Disease: Paraneoplastic Syndromes
Paraneoplastic Syndromes
group Neoplasms Neoplastic Process 28 0.010 None 1.000 1 2018 2018
CUI: C0497550
Disease: Benign neurologic neoplasms
Benign neurologic neoplasms
group Neoplasms; Nervous System Diseases Neoplastic Process 29 2 0.010 None 1.000 1 2012 2012
CUI: C0036631
Disease: Seminoma
Seminoma
disease Neoplasms Neoplastic Process 311 12 0.010 None < 0.001 1 2010 2010
Leukocyte adhesion deficiency type 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases Disease or Syndrome 114 26 0.010 None 1.000 1 2013 2013
CUI: C0403622
Disease: Primary vesicoureteric reflux
Primary vesicoureteric reflux
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Congenital Abnormality 8 1 0.010 None < 0.001 1 1 2009 2009
CUI: C0040250
Disease: Tinea Capitis
Tinea Capitis
disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 13 0.010 None 1.000 1 2004 2004
CUI: C0040156
Disease: Thyrotoxicosis
Thyrotoxicosis
disease Endocrine System Diseases Disease or Syndrome 37 7 0.010 None 1.000 1 2005 2005
CUI: C0406810
Disease: Carney Complex
Carney Complex
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Cardiovascular Diseases Disease or Syndrome 82 27 0.010 None 1.000 1 2012 2012
CUI: C0431564
Disease: Lobulated tongue
Lobulated tongue
disease Congenital Abnormality 14 0.010 None 1.000 1 2012 2012
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis
disease Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Disease or Syndrome 17 16 0.010 None 1.000 1 2011 2011
CUI: C0432306
Disease: Ichthyosis Bullosa of Siemens
Ichthyosis Bullosa of Siemens
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Congenital Abnormality 37 12 0.010 None 1.000 1 2018 2018
CUI: C0442874
Disease: Neuropathy
Neuropathy
group Nervous System Diseases Disease or Syndrome 484 110 0.010 None 1.000 1 2018 2018