DMP1, dentin matrix acidic phosphoprotein 1, 1758

N. diseases: 134; N. variants: 6
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.
Hantavirus infection in conditions classified elsewhere and of unspecified site
disease Disease or Syndrome 21 1 0.010 None 1.000 1 2020 2020
Hemorrhagic Fever with Renal Syndrome
disease Infections Disease or Syndrome 51 1 0.010 None 1.000 1 2020 2020
CUI: C0242490
Disease: Enthesopathy
Enthesopathy
disease Musculoskeletal Diseases; Wounds and Injuries Disease or Syndrome 11 1 0.010 None 1.000 1 2020 2020
CUI: C0242994
Disease: Hantavirus Infections
Hantavirus Infections
group Infections Disease or Syndrome 108 10 0.010 None 1.000 1 2020 2020
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases
group Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Disease or Syndrome 1074 306 0.040 None 1.000 4 2019 2019
CUI: C0005940
Disease: Bone Diseases
Bone Diseases
group Musculoskeletal Diseases Disease or Syndrome 317 10 0.020 None 1.000 2 2019 2020
CUI: C0020502
Disease: Hyperparathyroidism
Hyperparathyroidism
disease Endocrine System Diseases Disease or Syndrome 111 14 0.010 None 1.000 1 2019 2019
CUI: C0020550
Disease: Hyperthyroidism
Hyperthyroidism
disease Endocrine System Diseases Disease or Syndrome 279 27 0.010 None 1.000 1 2019 2019
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
disease Endocrine System Diseases Disease or Syndrome 613 283 0.010 None 1.000 1 2019 2019
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy
disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 403 67 0.010 None 1.000 1 2019 2019
CUI: C0376154
Disease: Skin callus
Skin callus
disease Skin and Connective Tissue Diseases Acquired Abnormality 154 0.010 None 1.000 1 2019 2019
CUI: C0011432
Disease: Dentin Sensitivity
Dentin Sensitivity
disease Stomatognathic Diseases Disease or Syndrome 19 0.010 None 1.000 1 2019 2019
CUI: C0025517
Disease: Metabolic Diseases
Metabolic Diseases
group Nutritional and Metabolic Diseases Disease or Syndrome 945 50 0.010 None 1.000 1 2019 2019
CUI: C0003864
Disease: Arthritis
Arthritis
disease Musculoskeletal Diseases Disease or Syndrome 1072 69 0.010 None 1.000 1 2019 2019
CUI: C0221002
Disease: Hyperparathyroidism, Primary
Hyperparathyroidism, Primary
disease Endocrine System Diseases Disease or Syndrome 115 39 0.010 None 1.000 1 2019 2019
CUI: C0332877
Disease: Congenital premature fusion
Congenital premature fusion
disease Congenital Abnormality 6 1 0.010 None 1.000 1 2019 2019
CUI: C0028259
Disease: Nodule
Nodule
phenotype Acquired Abnormality 278 19 0.020 None 1.000 2 2017 2019
Temporomandibular joint osteoarthritis
disease Disease or Syndrome 32 0.010 None 1.000 1 2017 2017
CUI: C0020492
Disease: Hyperostosis
Hyperostosis
disease Musculoskeletal Diseases Disease or Syndrome 50 3 0.010 None 1.000 1 2017 2017
CUI: C1881083
Disease: Hyperocclusion
Hyperocclusion
phenotype Stomatognathic Diseases Anatomical Abnormality 1 0.010 None 1.000 1 2017 2017
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 291 5 0.010 None 1.000 1 2017 2017
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases Disease or Syndrome 1189 238 0.010 None 1.000 1 2017 2017
CUI: C0012546
Disease: Diphtheria
Diphtheria
disease Infections Disease or Syndrome 147 0.010 None 1.000 1 2017 2017
CUI: C0598608
Disease: Hyperhomocysteinemia
Hyperhomocysteinemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 246 45 0.010 None 1.000 1 2017 2017
Diabetes Mellitus, Non-Insulin-Dependent
disease Nutritional and Metabolic Diseases; Endocrine System Diseases Disease or Syndrome 3134 2672 0.010 None 1.000 1 2017 2017