BTG3, BTG anti-proliferation factor 3, 10950

N. diseases: 141; N. variants: 0
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: C1290049
Disease: Plaque morphea
Plaque morphea 		disease Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 2006 2006
CUI: C4055160
Disease: Deep Circumscribed Morphea
Deep Circumscribed Morphea 		disease Disease or Syndrome 1 0.010 None 1.000 1 2006 2006
CUI: C0263664
Disease: Generalized morphea
Generalized morphea 		disease Skin and Connective Tissue Diseases Disease or Syndrome 3 0.010 None 1.000 1 2006 2006
CUI: C0406637
Disease: Erythema multiforme-like lupus erythematosus
Erythema multiforme-like lupus erythematosus 		disease Skin and Connective Tissue Diseases Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C1864497
Disease: PSORIASIS 2
PSORIASIS 2 		disease Disease or Syndrome 4 14 0.010 None 1.000 1 2016 2016
CUI: C0034931
Disease: Reflex Sympathetic Dystrophy
Reflex Sympathetic Dystrophy 		disease Nervous System Diseases Disease or Syndrome 5 0.010 None 1.000 1 2017 2017
CUI: C0263409
Disease: Linear Scleroderma
Linear Scleroderma 		disease Skin and Connective Tissue Diseases Disease or Syndrome 9 0.010 None 1.000 1 2006 2006
CUI: C0751506
Disease: REM Sleep Deprivation
REM Sleep Deprivation 		phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders Disease or Syndrome 9 0.010 None 1.000 1 2017 2017
CUI: C0853888
Disease: Hypocomplementaemia
Hypocomplementaemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 14 1 0.010 None 1.000 1 2018 2018
CUI: C0278080
Disease: Physical addiction
Physical addiction 		disease Chemically-Induced Disorders; Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 18 0.010 None 1.000 1 2018 2018
CUI: C1527383
Disease: Morphea
Morphea 		disease Skin and Connective Tissue Diseases Disease or Syndrome 20 0.010 None < 0.001 1 2017 2017
CUI: C0270726
Disease: Alexander Disease
Alexander Disease 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases Disease or Syndrome 27 99 0.010 None 1.000 1 2019 2019
CUI: C1290344
Disease: Nonspecific interstitial pneumonia
Nonspecific interstitial pneumonia 		disease Respiratory Tract Diseases Disease or Syndrome 28 1 0.010 None 1.000 1 2018 2018
CUI: C0020455
Disease: Hypergammaglobulinemia
Hypergammaglobulinemia 		disease Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 36 0.010 None 1.000 1 2018 2018
CUI: C0010403
Disease: Cryoglobulinemia
Cryoglobulinemia 		disease Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 37 7 0.010 None 1.000 1 2016 2016
CUI: C0014742
Disease: Erythema Multiforme
Erythema Multiforme 		disease Skin and Connective Tissue Diseases Disease or Syndrome 38 2 0.010 None 1.000 1 2019 2019
CUI: C0036420
Disease: Localized scleroderma
Localized scleroderma 		disease Skin and Connective Tissue Diseases Disease or Syndrome 51 0.010 None < 0.001 1 2017 2017
CUI: C0042165
Disease: Anterior uveitis
Anterior uveitis 		disease Eye Diseases Disease or Syndrome 53 20 0.010 None 1.000 1 2006 2006
CUI: C1258104
Disease: Diffuse Scleroderma
Diffuse Scleroderma 		disease Skin and Connective Tissue Diseases Disease or Syndrome 56 5 0.010 None 1.000 1 2018 2018
CUI: C1384494
Disease: Metastatic Carcinoma
Metastatic Carcinoma 		group Pathological Conditions, Signs and Symptoms; Neoplasms Neoplastic Process 57 2 0.010 None 1.000 1 2013 2013
CUI: C0026272
Disease: Mixed Connective Tissue Disease
Mixed Connective Tissue Disease 		disease Skin and Connective Tissue Diseases Disease or Syndrome 61 4 0.010 None 1.000 1 2019 2019
CUI: C0034735
Disease: Raynaud Phenomenon
Raynaud Phenomenon 		disease Cardiovascular Diseases Disease or Syndrome 63 1 0.010 None 1.000 1 2018 2018
CUI: C1832588
Disease: Chromosome 11p11.2 Deletion Syndrome
Chromosome 11p11.2 Deletion Syndrome 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases Disease or Syndrome 65 6 0.010 None 1.000 1 2018 2018
CUI: C0311370
Disease: Lupus anticoagulant disorder
Lupus anticoagulant disorder 		disease Pathological Conditions, Signs and Symptoms; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 66 14 0.020 None 1.000 2 2019 2019
CUI: C1849193
Disease: PEELING SKIN SYNDROME
PEELING SKIN SYNDROME 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases Disease or Syndrome 67 11 0.010 None 1.000 1 2018 2018