BMPER, BMP binding endothelial regulator, 168667

N. diseases: 75; 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: C1842691
Disease: Diaphanospondylodysostosis
Diaphanospondylodysostosis
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Disease or Syndrome 1 4 0.730 strong 1.000 4 4 2010 2019
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
disease Digestive System Diseases; Neoplasms Neoplastic Process 5725 942 0.310 None 1.000 2 1997 2017
CUI: C0524662
Disease: Opiate Addiction
Opiate Addiction
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 81 46 0.300 None 1.000 1 2008 2008
CUI: C0027412
Disease: Opioid-Related Disorders
Opioid-Related Disorders
group Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 12 23 0.300 None 1.000 1 2008 2008
CUI: C0029095
Disease: Opioid abuse
Opioid abuse
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 16 0.300 None 1.000 1 2008 2008
CUI: C4551628
Disease: Opiate Abuse
Opiate Abuse
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 12 0.300 None 1.000 1 2008 2008
CUI: C0524661
Disease: Narcotic Abuse
Narcotic Abuse
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 6 0.300 None 1.000 1 2008 2008
CUI: C1527402
Disease: Narcotic Dependence
Narcotic Dependence
disease Chemically-Induced Disorders; Mental Disorders Mental or Behavioral Dysfunction 7 1 0.300 None 1.000 1 2008 2008
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
disease Digestive System Diseases; Infections Disease or Syndrome 1768 347 0.100 None 1.000 68 1992 2020
CUI: C0042834
Disease: Vital capacity
Vital capacity
phenotype Clinical Attribute 430 746 0.100 None 1.000 1 1 2019 2019
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
disease Nervous System Diseases; Mental Disorders Disease or Syndrome 3397 1843 0.100 None 1.000 1 6 2014 2014
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function
phenotype Organ or Tissue Function 272 1169 0.100 None 1.000 1 1 2015 2015
CUI: C1836542
Disease: Depressed nasal bridge
Depressed nasal bridge
phenotype Finding 426 39 0.100 None 0
CUI: C1834931
Disease: Cystic renal dysplasia
Cystic renal dysplasia
disease Anatomical Abnormality 12 4 0.100 None 0
Abnormal vertebral segmentation and fusion
disease Anatomical Abnormality 11 0.100 None 0
Absent or minimally ossified vertebral bodies
phenotype Finding 9 0.100 None 0
Absent in utero ossification of vertebral bodies
phenotype Finding 1 0.100 None 0
CUI: C1320468
Disease: Nephrogenic rest
Nephrogenic rest
disease Anatomical Abnormality 15 0.100 None 0
CUI: C1136179
Disease: Hammer Toe
Hammer Toe
phenotype Musculoskeletal Diseases Anatomical Abnormality 46 11 0.100 None 0
CUI: C0948187
Disease: Tracheomalacia
Tracheomalacia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Respiratory Tract Diseases Disease or Syndrome 30 5 0.100 None 0
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus
disease Congenital Abnormality 417 30 0.100 None 0
CUI: C0557874
Disease: Global developmental delay
Global developmental delay
disease Mental or Behavioral Dysfunction 1825 553 0.100 None 0
CUI: C0542518
Disease: Enlarged kidney
Enlarged kidney
phenotype Finding 27 2 0.100 None 0
CUI: C1837482
Disease: Thoracic hypoplasia
Thoracic hypoplasia
disease Congenital Abnormality 32 16 0.100 None 0
CUI: C4023676
Disease: Increased nuchal translucency
Increased nuchal translucency
phenotype Pathological Conditions, Signs and Symptoms Finding 30 2 0.100 None 0