GDNF, glial cell derived neurotrophic factor, 2668

N. diseases: 409; N. variants: 13
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: C1274923
Disease: Cutaneous hyperalgesia
Cutaneous hyperalgesia 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 1 0.010 None 1.000 1 2017 2017
CUI: C3150974
Disease: HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3 		disease Finding 2 4 0.600 moderate 1.000 5 4 1996 2002
CUI: C0013375
Disease: Dysganglionosis
Dysganglionosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 2 0.010 None 1.000 1 1998 1998
CUI: C1275047
Disease: Radiation-induced xerostomia
Radiation-induced xerostomia 		disease Stomatognathic Diseases Disease or Syndrome 2 1 0.010 None 1.000 1 2014 2014
CUI: C2939445
Disease: Carcinoma in situ of bronchus
Carcinoma in situ of bronchus 		disease Neoplasms; Respiratory Tract Diseases Neoplastic Process 2 0.010 None 1.000 1 2005 2005
CUI: C4020790
Disease: Medullary sponge kidney disease
Medullary sponge kidney disease 		disease Disease or Syndrome 2 0.010 None 1.000 1 2010 2010
CUI: C4520773
Disease: Stage 0 Lung Cancer AJCC v6 and v7
Stage 0 Lung Cancer AJCC v6 and v7 		disease Neoplasms Neoplastic Process 2 0.010 None 1.000 1 2005 2005
CUI: C1399358
Disease: Hemiparkinsonism
Hemiparkinsonism 		disease Disease or Syndrome 4 0.010 None 1.000 1 2006 2006
CUI: C4316837
Disease: Clear cell odontogenic carcinoma
Clear cell odontogenic carcinoma 		disease Neoplastic Process 4 0.010 None 1.000 1 2015 2015
CUI: C0238707
Disease: Impairment of attention
Impairment of attention 		disease Mental or Behavioral Dysfunction 5 0.010 None 1.000 1 2020 2020
CUI: C0334578
Disease: Papillary ependymoma
Papillary ependymoma 		disease Neoplasms Neoplastic Process 6 0.300 None 1.000 1 2009 2009
CUI: C0422837
Disease: Neurological observations
Neurological observations 		group Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 6 0.300 None 1.000 1 2010 2010
CUI: C0546275
Disease: Hypoganglionosis
Hypoganglionosis 		disease Disease or Syndrome 6 1 0.010 None 1.000 1 2001 2001
CUI: C0746857
Disease: Focal Neurologic Deficits
Focal Neurologic Deficits 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 6 0.300 None 1.000 1 2010 2010
CUI: C0751377
Disease: Neurologic Dysfunction
Neurologic Dysfunction 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 6 0.300 None 1.000 1 2010 2010
CUI: C4543822
Disease: Gaming disorder
Gaming disorder 		disease Mental Disorders Mental or Behavioral Dysfunction 6 2 0.010 None 1.000 1 2019 2019
CUI: C0344461
Disease: Oligodendroblastoma
Oligodendroblastoma 		disease Neoplasms Neoplastic Process 7 0.300 None 1.000 1 2009 2009
CUI: C0751395
Disease: Mixed Oligodendroglioma-Ependymoma
Mixed Oligodendroglioma-Ependymoma 		disease Neoplasms Neoplastic Process 7 0.300 None 1.000 1 2009 2009
CUI: C1384403
Disease: Cellular Ependymoma
Cellular Ependymoma 		disease Neoplasms Neoplastic Process 7 0.300 None 1.000 1 2009 2009
CUI: C1859049
Disease: CCHS WITH HIRSCHSPRUNG DISEASE
CCHS WITH HIRSCHSPRUNG DISEASE 		disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases Disease or Syndrome; Congenital Abnormality 7 1 0.300 None 1.000 1 1998 1998
CUI: C0521654
Disease: Neurologic Deficits
Neurologic Deficits 		group Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 8 4 0.300 None 1.000 1 2010 2010
CUI: C1707516
Disease: Corneal Sensitivity
Corneal Sensitivity 		phenotype Sign or Symptom 8 0.010 None 1.000 1 2017 2017
CUI: C1857175
Disease: Episodic hypertension
Episodic hypertension 		phenotype Cardiovascular Diseases Finding 8 0.100 None 0
CUI: C0022681
Disease: Medullary sponge kidney
Medullary sponge kidney 		disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome; Congenital Abnormality 9 3 0.040 None 1.000 4 2010 2017
CUI: C0403477
Disease: Medullary nephrocalcinosis
Medullary nephrocalcinosis 		disease Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 9 2 0.010 None 1.000 1 2018 2018