PRG4, proteoglycan 4, 10216

N. diseases: 73; N. variants: 1
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: C1393871
Disease: Congenital finger flexion contractures
Congenital finger flexion contractures 		disease Congenital Abnormality 5 1 0.100 None 0
CUI: C0409345
Disease: Flexion contracture - wrist
Flexion contracture - wrist 		disease Acquired Abnormality 15 4 0.100 None 0
CUI: C0410574
Disease: Synovial Hypertrophy
Synovial Hypertrophy 		disease Musculoskeletal Diseases Disease or Syndrome 12 0.100 None 0
CUI: C0031048
Disease: Pericarditis, Constrictive
Pericarditis, Constrictive 		disease Cardiovascular Diseases Disease or Syndrome 8 1 0.100 None 0
CUI: C4023134
Disease: Flattened metacarpal heads
Flattened metacarpal heads 		disease Anatomical Abnormality 1 0.100 None 0
CUI: C4025238
Disease: Generalized morning stiffness
Generalized morning stiffness 		phenotype Finding 2 1 0.100 None 0
CUI: C4025240
Disease: Flattened metatarsal heads
Flattened metatarsal heads 		disease Anatomical Abnormality 2 0.100 None 0
CUI: C0239138
Disease: Hip joint varus deformity - observation
Hip joint varus deformity - observation 		phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Finding 49 2 0.100 None 0
CUI: C0020507
Disease: Hyperplasia
Hyperplasia 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 131 0.300 None 1.000 1 1999 1999
CUI: C1167732
Disease: Pleuropericarditis
Pleuropericarditis 		disease Cardiovascular Diseases Disease or Syndrome 1 0.300 None 1.000 1 1999 1999
CUI: C0009917
Disease: Contracture
Contracture 		disease Musculoskeletal Diseases Anatomical Abnormality 111 12 0.300 None 1.000 1 1999 1999
CUI: C0031046
Disease: Pericarditis
Pericarditis 		disease Cardiovascular Diseases Disease or Syndrome 51 6 0.300 None 1.000 1 1999 1999
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		disease Musculoskeletal Diseases Disease or Syndrome 368 150 0.010 None 1.000 1 2007 2007
CUI: C0039730
Disease: Thalassemia
Thalassemia 		group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 136 18 0.010 None 1.000 1 2018 2018
CUI: C0403414
Disease: Acute post-streptococcal glomerulonephritis
Acute post-streptococcal glomerulonephritis 		disease Female Urogenital Diseases and Pregnancy Complications; Infections; Male Urogenital Diseases Disease or Syndrome 7 0.010 None 1.000 1 2018 2018
CUI: C0314719
Disease: Dryness of eye
Dryness of eye 		phenotype Eye Diseases Sign or Symptom 149 1 0.010 None 1.000 1 2017 2017
CUI: C0279644
Disease: Childhood Acute Myelomonocytic Leukemia
Childhood Acute Myelomonocytic Leukemia 		disease Neoplasms Neoplastic Process 28 3 0.010 None 1.000 1 2002 2002
CUI: C0279627
Disease: Adult Acute Myelomonocytic Leukemia
Adult Acute Myelomonocytic Leukemia 		disease Neoplasms Neoplastic Process 28 3 0.010 None 1.000 1 2002 2002
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance 		phenotype Nutritional and Metabolic Diseases Disease or Syndrome 596 81 0.010 None 1.000 1 2019 2019
CUI: C0243026
Disease: Sepsis
Sepsis 		disease Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 1453 144 0.010 None 1.000 1 2020 2020
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias 		group Nutritional and Metabolic Diseases Disease or Syndrome 471 184 0.010 None 1.000 1 2019 2019
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease 		disease Disease or Syndrome 741 81 0.010 None 1.000 1 2019 2019
CUI: C0549523
Disease: Oropharynx (excludes nasopharynx)
Oropharynx (excludes nasopharynx) 		disease Disease or Syndrome 94 5 0.010 None 1.000 1 2018 2018
CUI: C3495890
Disease: Osteochondral defects
Osteochondral defects 		phenotype Anatomical Abnormality 17 0.010 None 1.000 1 2018 2018
CUI: C2894027
Disease: Post traumatic osteoarthritis
Post traumatic osteoarthritis 		disease Disease or Syndrome 22 0.010 None 1.000 1 2019 2019