SNURF, SNRPN upstream reading frame, 8926

N. diseases: 63; N. variants: 1
Source: BEFREE ×
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: C0917981
Disease: Progressive Muscular Atrophy
Progressive Muscular Atrophy
disease Nervous System Diseases Disease or Syndrome 15 1 0.010 None 1.000 1 2013 2013
CUI: C0014060
Disease: Encephalitis, St. Louis
Encephalitis, St. Louis
disease Infections; Nervous System Diseases Disease or Syndrome 272 34 0.010 None 1.000 1 1994 1994
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma
disease Neoplasms; Nervous System Diseases Neoplastic Process 2419 231 0.010 None 1.000 1 2014 2014
CUI: C0553580
Disease: Ewings sarcoma
Ewings sarcoma
disease Neoplasms Neoplastic Process 511 12 0.010 None 1.000 1 2003 2003
CUI: C0017665
Disease: Membranous glomerulonephritis
Membranous glomerulonephritis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Immune System Diseases Disease or Syndrome 152 12 0.010 None < 0.001 1 2019 2019
CUI: C0442874
Disease: Neuropathy
Neuropathy
group Nervous System Diseases Disease or Syndrome 477 75 0.010 None 1.000 1 1997 1997
CUI: C1511934
Disease: Differentiating Neuroblastoma
Differentiating Neuroblastoma
disease Neoplasms Neoplastic Process 20 0.010 None 1.000 1 2009 2009
CUI: C1535926
Disease: Neurodevelopmental Disorders
Neurodevelopmental Disorders
group Mental Disorders Mental or Behavioral Dysfunction 485 10 0.010 None 1.000 1 2012 2012
CUI: C0004114
Disease: Astrocytoma
Astrocytoma
disease Neoplasms Neoplastic Process 958 51 0.010 None 1.000 1 2012 2012
CUI: C0004936
Disease: Mental disorders
Mental disorders
group Mental Disorders Mental or Behavioral Dysfunction 763 101 0.010 None 1.000 1 2012 2012
CUI: C3489532
Disease: Cone-Rod Dystrophy 2
Cone-Rod Dystrophy 2
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 247 48 0.010 None 1.000 1 2009 2009
CUI: C3266262
Disease: Multiple Chronic Conditions
Multiple Chronic Conditions
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 929 42 0.010 None 1.000 1 2016 2016
CUI: C1954751
Disease: Microdeletion syndromes
Microdeletion syndromes
disease Disease or Syndrome 18 0.010 None 1.000 1 2012 2012
CUI: C1865384
Disease: Amyotrophy, monomelic
Amyotrophy, monomelic
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 15 2 0.010 None 1.000 1 2005 2005
Heredodegenerative Disorders, Nervous System
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome 15 0.010 None 1.000 1 2008 2008
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
disease Disease or Syndrome 1075 276 0.010 None 1.000 1 2015 2015
CUI: C0410158
Disease: Muscle damage
Muscle damage
phenotype Acquired Abnormality 163 4 0.010 None 1.000 1 2014 2014
CUI: C0278704
Disease: Malignant Childhood Neoplasm
Malignant Childhood Neoplasm
disease Neoplasms Neoplastic Process 174 20 0.010 None 1.000 1 2019 2019
CUI: C0270765
Disease: Myelopathic Muscular Atrophy
Myelopathic Muscular Atrophy
disease Nervous System Diseases Disease or Syndrome 6 0.010 None 1.000 1 1996 1996
CUI: C0027651
Disease: Neoplasms
Neoplasms
group Neoplasms Neoplastic Process 10153 1571 0.010 None 1.000 1 2009 2009
CUI: C0042133
Disease: Uterine Fibroids
Uterine Fibroids
group Neoplasms Neoplastic Process 528 52 0.010 None 1.000 1 1996 1996
CUI: C0027819
Disease: Neuroblastoma
Neuroblastoma
disease Neoplasms Neoplastic Process 2469 234 0.010 None 1.000 1 2014 2014
CUI: C0036631
Disease: Seminoma
Seminoma
disease Neoplasms Neoplastic Process 290 11 0.010 None < 0.001 1 2018 2018
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
disease Mental Disorders Mental or Behavioral Dysfunction 2217 1332 0.010 None 1.000 1 2018 2018
CUI: C0028754
Disease: Obesity
Obesity
disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 2459 900 0.010 None 1.000 1 2017 2017