MUC1, mucin 1, cell surface associated, 4582

N. diseases: 594; N. variants: 18
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: C1858395
Disease: Tubular atrophy
Tubular atrophy
phenotype Finding 17 1 0.100 None 0
Tubular basement membrane disintegration
phenotype Finding 4 0.100 None 0
CUI: C0700225
Disease: Serum creatinine raised
Serum creatinine raised
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Finding 27 2 0.100 None 0
CUI: C1968619
Disease: Renal corticomedullary cysts
Renal corticomedullary cysts
disease Disease or Syndrome 8 0.100 None 0
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy
disease Disease or Syndrome 271 13 0.100 None 0
CUI: C1969371
Disease: Impaired renal uric acid clearance
Impaired renal uric acid clearance
phenotype Finding 1 0.100 None 0
CUI: C0178664
Disease: Glomerulosclerosis (disorder)
Glomerulosclerosis (disorder)
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases Disease or Syndrome 221 3 0.100 None 0
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormality 96 8 0.100 None 0
CUI: C0020649
Disease: Hypotension
Hypotension
phenotype Cardiovascular Diseases Finding 125 2 0.100 None 0
CUI: C1846347
Disease: Renal salt wasting
Renal salt wasting
phenotype Finding 22 0.100 None 0
Decreased glomerular filtration rate
phenotype Finding 11 0.100 None 0
CUI: C4521759
Disease: Tubular Atrophy Assessment
Tubular Atrophy Assessment
phenotype Diagnostic Procedure 17 0.100 None 0
CUI: C4025730
Disease: Renal cortical atrophy
Renal cortical atrophy
disease Disease or Syndrome 1 0.100 None 0
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
group Cardiovascular Diseases Disease or Syndrome 2322 1085 0.100 None 0
CUI: C0017658
Disease: Glomerulonephritis
Glomerulonephritis
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 391 7 0.100 None 0
MiT family translocation renal cell carcinoma
disease Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 33 0.010 None < 0.001 1 2010 2010
CUI: C1302401
Disease: Adenoma of large intestine
Adenoma of large intestine
disease Digestive System Diseases; Neoplasms Neoplastic Process 452 213 0.010 None < 0.001 1 2002 2002
CUI: C3672440
Disease: Bile duct hyperplasia
Bile duct hyperplasia
disease Disease or Syndrome 9 0.010 None < 0.001 1 2019 2019
CUI: C2826323
Disease: Refractory Cytopenia of Childhood
Refractory Cytopenia of Childhood
disease Neoplastic Process 264 3 0.010 None < 0.001 1 2010 2010
CUI: C0279651
Disease: Gallbladder adenocarcinoma
Gallbladder adenocarcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 53 2 0.010 None < 0.001 1 2017 2017
Newly Diagnosed Childhood Ependymoma
disease Neoplasms Neoplastic Process 144 3 0.010 None < 0.001 1 2015 2015
CUI: C0334263
Disease: Trichilemmoma
Trichilemmoma
disease Neoplasms Neoplastic Process 8 4 0.010 None < 0.001 1 2018 2018
CUI: C0278874
Disease: Adult Ependymoma
Adult Ependymoma
disease Neoplasms Neoplastic Process 144 3 0.010 None < 0.001 1 2015 2015
CUI: C4552766
Disease: Miscarriage
Miscarriage
disease Female Urogenital Diseases and Pregnancy Complications Disease or Syndrome 426 56 0.010 None < 0.001 1 2018 2018
CUI: C0205788
Disease: Histiocytoid hemangioma
Histiocytoid hemangioma
disease Neoplasms Neoplastic Process 18 1 0.010 None < 0.001 1 2019 2019