BMP2, bone morphogenetic protein 2, 650

N. diseases: 428; N. variants: 12
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: C0085681
Disease: Hyperphosphatemia (disorder)
Hyperphosphatemia (disorder)
disease Nutritional and Metabolic Diseases Disease or Syndrome 65 1 0.010 None 1.000 1 2019 2019
CUI: C0037930
Disease: Spinal Cord Neoplasms
Spinal Cord Neoplasms
group Neoplasms; Nervous System Diseases Neoplastic Process 27 1 0.010 None 1.000 1 2018 2018
CUI: C0036631
Disease: Seminoma
Seminoma
disease Neoplasms Neoplastic Process 311 12 0.010 None 1.000 1 2008 2008
CUI: C0029429
Disease: Osteochondrosis
Osteochondrosis
disease Musculoskeletal Diseases Disease or Syndrome 9 0.010 None 1.000 1 2018 2018
CUI: C0029423
Disease: Cartilaginous exostosis
Cartilaginous exostosis
disease Neoplasms; Musculoskeletal Diseases Neoplastic Process 47 2 0.010 None 1.000 1 2001 2001
CUI: C0029422
Disease: Osteochondrodysplasias
Osteochondrodysplasias
group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 207 26 0.010 None 1.000 1 2014 2014
CUI: C0028880
Disease: Odontogenic Tumors
Odontogenic Tumors
group Neoplasms Neoplastic Process 62 2 0.010 None 1.000 1 2017 2017
CUI: C0028840
Disease: Ocular Hypertension
Ocular Hypertension
disease Eye Diseases Disease or Syndrome 103 8 0.010 None 1.000 1 2014 2014
CUI: C0028756
Disease: Obesity, Morbid
Obesity, Morbid
disease Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases Disease or Syndrome 203 49 0.010 None 1.000 1 2016 2016
CUI: C0027708
Disease: Nephroblastoma
Nephroblastoma
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Neoplastic Process 586 125 0.010 None 1.000 1 2015 2015
CUI: C1969372
Disease: Tubulointerstitial fibrosis
Tubulointerstitial fibrosis
phenotype Disease or Syndrome 328 0.010 None 1.000 1 2009 2009
CUI: C0027543
Disease: Avascular necrosis of bone
Avascular necrosis of bone
phenotype Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Disease or Syndrome 73 5 0.010 None 1.000 1 2014 2014
CUI: C0026936
Disease: Mycoplasma Infections
Mycoplasma Infections
group Infections Disease or Syndrome 188 1 0.010 None 1.000 1 2008 2008
CUI: C2350038
Disease: Molar Incisor Hypomineralization
Molar Incisor Hypomineralization
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases Disease or Syndrome 7 4 0.010 None 1.000 1 2019 2019
CUI: C1956089
Disease: Osteophyte
Osteophyte
disease Musculoskeletal Diseases Disease or Syndrome 91 0.010 None 1.000 1 2018 2018
CUI: C1861329
Disease: Spinal canal stenosis
Spinal canal stenosis
disease Musculoskeletal Diseases Anatomical Abnormality 35 0.010 None 1.000 1 2017 2017
CUI: C0030193
Disease: Pain
Pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 1554 196 0.010 None 1.000 1 2019 2019
CUI: C0035934
Disease: Rubinstein-Taybi Syndrome
Rubinstein-Taybi Syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 31 88 0.010 None 1.000 1 2012 2012
CUI: C0035851
Disease: Root Resorption
Root Resorption
disease Stomatognathic Diseases Disease or Syndrome 43 7 0.010 None 1.000 1 2008 2008
CUI: C0035412
Disease: Rhabdomyosarcoma
Rhabdomyosarcoma
disease Neoplasms Neoplastic Process 565 20 0.010 None 1.000 1 2014 2014
Prieto X-linked mental retardation syndrome
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 16 0.010 None 1.000 1 2019 2019
CUI: C0032915
Disease: Preexcitation Syndrome
Preexcitation Syndrome
disease Cardiovascular Diseases Disease or Syndrome 20 2 0.010 None 1.000 1 2012 2012
CUI: C0340100
Disease: High altitude pulmonary edema
High altitude pulmonary edema
disease Respiratory Tract Diseases Disease or Syndrome 56 45 0.010 None 1.000 1 2016 2016
CUI: C0032002
Disease: Pituitary Diseases
Pituitary Diseases
group Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 153 3 0.010 None 1.000 1 2017 2017
Miller-McKusick-Malvaux-Syndrome (3M Syndrome)
disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases Disease or Syndrome 11 11 0.010 None 1.000 1 2019 2019