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: C1968619
Disease: Renal corticomedullary cysts
Renal corticomedullary cysts
disease Disease or Syndrome 8 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: C0020538
Disease: Hypertensive disease
Hypertensive disease
group Cardiovascular Diseases Disease or Syndrome 2322 1085 0.100 None 0
CUI: C0020649
Disease: Hypotension
Hypotension
phenotype Cardiovascular Diseases Finding 125 2 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: 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: 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: C1969371
Disease: Impaired renal uric acid clearance
Impaired renal uric acid clearance
phenotype Finding 1 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: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy
disease Disease or Syndrome 271 13 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
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
Adult Diffuse Large B-Cell Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 504 46 0.010 None 1.000 1 1992 1992
CUI: C0032584
Disease: polyps
polyps
phenotype Pathological Conditions, Signs and Symptoms Anatomical Abnormality 390 18 0.010 None 1.000 1 1993 1993
CUI: C0206677
Disease: Adenomatous Polyps
Adenomatous Polyps
disease Neoplasms Neoplastic Process 120 20 0.010 None 1.000 1 1996 1996
CUI: C1334425
Disease: Low Grade Malignant Neoplasm
Low Grade Malignant Neoplasm
disease Neoplastic Process 1 0.010 None 1.000 1 1996 1996
CUI: C1879344
Disease: Biliary papillomatosis
Biliary papillomatosis
disease Digestive System Diseases; Neoplasms Neoplastic Process 20 0.010 None 1.000 1 1996 1996
CUI: C0004114
Disease: Astrocytoma
Astrocytoma
disease Neoplasms Neoplastic Process 985 59 0.010 None 1.000 1 1997 1997
CUI: C0007133
Disease: Carcinoma, Papillary
Carcinoma, Papillary
disease Neoplasms Neoplastic Process 225 9 0.010 None 1.000 1 1997 1997
CUI: C0035460
Disease: Rhinitis, Vasomotor
Rhinitis, Vasomotor
disease Respiratory Tract Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 2 0.010 None 1.000 1 1997 1997
CUI: C4086152
Disease: Childhood Astrocytoma
Childhood Astrocytoma
disease Neoplasms Neoplastic Process 615 39 0.010 None 1.000 1 1997 1997
CUI: C1855681
Disease: Nephronophthisis, familial juvenile
Nephronophthisis, familial juvenile
disease Disease or Syndrome 17 0.010 None 1.000 1 1998 1998