PLF, Pulmonary function, 450095

N. diseases: 124; 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: C2931591
Disease: Juvenile systemic scleroderma
Juvenile systemic scleroderma
disease Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C1565249
Disease: Mobility Limitation
Mobility Limitation
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 3 0.010 None 1.000 1 2018 2018
CUI: C0694548
Disease: Cough variant asthma
Cough variant asthma
disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C0854076
Disease: Distal ileal obstruction syndrome
Distal ileal obstruction syndrome
disease Disease or Syndrome 4 2 0.010 None 1.000 1 2004 2004
CUI: C4551465
Disease: Small airways disease
Small airways disease
disease Disease or Syndrome 4 0.010 None 1.000 1 2019 2019
CUI: C0149983
Disease: Lumbar spondylosis
Lumbar spondylosis
disease Musculoskeletal Diseases Disease or Syndrome 5 0.010 None 1.000 1 2018 2018
CUI: C0264184
Disease: Degenerative spondylolisthesis
Degenerative spondylolisthesis
disease Musculoskeletal Diseases Disease or Syndrome 7 0.010 None 1.000 1 2018 2018
CUI: C0546483
Disease: Lung cyst
Lung cyst
disease Pathological Conditions, Signs and Symptoms; Neoplasms; Respiratory Tract Diseases Disease or Syndrome 9 0.010 None < 0.001 1 2020 2020
CUI: C2051831
Disease: Pectus excavatum
Pectus excavatum
disease Musculoskeletal Diseases; Respiratory Tract Diseases Anatomical Abnormality 12 1 0.010 None 1.000 1 2018 2018
CUI: C1761609
Disease: Aspiration pneumonitis
Aspiration pneumonitis
disease Infections; Respiratory Tract Diseases Disease or Syndrome 13 0.010 None 1.000 1 2017 2017
CUI: C0038017
Disease: Congenital spondylolisthesis
Congenital spondylolisthesis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 17 1 0.020 None 1.000 2 2018 2019
CUI: C0238441
Disease: Subglottic stenosis
Subglottic stenosis
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases Anatomical Abnormality 17 2 0.010 None 1.000 1 2018 2018
CUI: C0030293
Disease: Pancreatic Insufficiency
Pancreatic Insufficiency
disease Digestive System Diseases Disease or Syndrome 21 23 0.010 None 1.000 1 2004 2004
Congenital bilateral aplasia of vas deferens
disease Male Urogenital Diseases Congenital Abnormality 27 210 0.010 None 1.000 1 1996 1996
CUI: C0038016
Disease: Spondylolisthesis
Spondylolisthesis
disease Musculoskeletal Diseases Disease or Syndrome 28 1 0.020 None 1.000 2 2018 2019
CUI: C0026707
Disease: Mucopolysaccharidosis IV
Mucopolysaccharidosis IV
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 28 9 0.010 None 1.000 1 1975 1975
CUI: C0007859
Disease: Neck Pain
Neck Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 29 3 0.010 None 1.000 1 2017 2017
CUI: C3161174
Disease: Hemoglobin H Disease
Hemoglobin H Disease
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 29 0.010 None 1.000 1 2005 2005
CUI: C0032290
Disease: Aspiration Pneumonia
Aspiration Pneumonia
disease Infections; Respiratory Tract Diseases Disease or Syndrome 32 4 0.010 None 1.000 1 2017 2017
CUI: C0149651
Disease: Clubbing
Clubbing
phenotype Sign or Symptom 32 1 0.010 None 1.000 1 2018 2018
CUI: C0877430
Disease: Asthma chronic
Asthma chronic
disease Disease or Syndrome 36 0.010 None 1.000 1 2018 2018
CUI: C1851100
Disease: LAURIN-SANDROW SYNDROME
LAURIN-SANDROW SYNDROME
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 36 0.010 None < 0.001 1 2019 2019
CUI: C0206525
Disease: Tuberculosis, Drug-Resistant
Tuberculosis, Drug-Resistant
disease Infections Disease or Syndrome 37 0.010 None 1.000 1 2019 2019
Obstructive sleep apnea hypopnea syndrome
disease Disease or Syndrome 41 7 0.010 None 1.000 1 2019 2019
Hereditary hemorrhagic telangiectasia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 42 81 0.010 None 1.000 1 2019 2019