MUC1, mucin 1, cell surface associated, 4582

N. diseases: 552; N. variants: 18
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: C0030805
Disease: Bullous pemphigoid
Bullous pemphigoid
disease Skin and Connective Tissue Diseases; Immune System Diseases Disease or Syndrome 119 9 0.010 None 1.000 1 2020 2020
CUI: C1368019
Disease: Paget Disease
Paget Disease
disease Neoplasms Neoplastic Process 60 5 0.010 None 1.000 1 2020 2020
CUI: C0003864
Disease: Arthritis
Arthritis
disease Musculoskeletal Diseases Disease or Syndrome 992 66 0.010 None 1.000 1 2020 2020
CUI: C0029401
Disease: Osteitis Deformans
Osteitis Deformans
disease Musculoskeletal Diseases Disease or Syndrome 127 45 0.010 None 1.000 1 2020 2020
CUI: C4290046
Disease: trachomatis
trachomatis
disease Disease or Syndrome 175 7 0.010 None 1.000 1 2020 2020
CUI: C0085077
Disease: Sweet Syndrome
Sweet Syndrome
disease Skin and Connective Tissue Diseases Disease or Syndrome 103 3 0.010 None 1.000 1 2020 2020
CUI: C0264733
Disease: Ventricular dilatation (disorder)
Ventricular dilatation (disorder)
disease Cardiovascular Diseases Disease or Syndrome 13 0.010 None 1.000 1 2020 2020
CUI: C0086981
Disease: Sicca Syndrome
Sicca Syndrome
disease Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases Disease or Syndrome 105 4 0.010 None 1.000 1 2020 2020
Childhood Anaplastic Large Cell Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 130 2 0.010 None 1.000 1 2020 2020
Adult Anaplastic Large Cell Lymphoma
disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases Neoplastic Process 128 2 0.010 None 1.000 1 2020 2020
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME
group Hemic and Lymphatic Diseases Neoplastic Process 975 79 0.020 None 1.000 2 2019 2019
CUI: C0278804
Disease: Adenocarcinoma of duodenum
Adenocarcinoma of duodenum
disease Digestive System Diseases; Neoplasms Neoplastic Process 8 0.020 None 0.500 2 2019 2019
Metastatic castration-resistant prostate cancer
disease Neoplastic Process 140 2 0.020 None 1.000 2 2019 2019
CUI: C0026847
Disease: Spinal Muscular Atrophy
Spinal Muscular Atrophy
disease Nervous System Diseases Disease or Syndrome 308 25 0.020 None 1.000 2 2019 2019
CUI: C0009782
Disease: Connective Tissue Diseases
Connective Tissue Diseases
group Skin and Connective Tissue Diseases Disease or Syndrome 168 14 0.020 None 1.000 2 2019 2019
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
group Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 2650 714 0.010 None 1.000 1 2019 2019
M5b Acute differentiated monocytic leukemia
disease Neoplasms; Hemic and Lymphatic Diseases Neoplastic Process 122 0.010 None 1.000 1 2019 2019
CUI: C0027121
Disease: Myositis
Myositis
disease Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 187 3 0.010 None 1.000 1 2019 2019
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 360 6 0.010 None 1.000 1 2019 2019
CUI: C1841972
Disease: Glucocorticoid Receptor Deficiency
Glucocorticoid Receptor Deficiency
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 104 6 0.010 None 1.000 1 2019 2019
CUI: C0027070
Disease: Myoepithelioma
Myoepithelioma
disease Neoplasms Neoplastic Process 35 0.010 None 1.000 1 2019 2019
CUI: C0010246
Disease: Coxsackievirus Infections
Coxsackievirus Infections
group Infections Disease or Syndrome 42 1 0.010 None 1.000 1 2019 2019
Polycystic Kidney, Autosomal Dominant
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 269 20 0.010 None 1.000 1 2019 2019
CUI: C0231341
Disease: Premature aging syndrome
Premature aging syndrome
disease Pathological Conditions, Signs and Symptoms Disease or Syndrome 134 5 0.010 None 1.000 1 2019 2019
CUI: C1636149
Disease: Macular dystrophy, corneal type 1
Macular dystrophy, corneal type 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Disease or Syndrome 100 24 0.010 None 1.000 1 2019 2019