ALB, albumin, 213

N. diseases: 1198; N. variants: 21
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: C4305253
Disease: Congenital analbuminemia
Congenital analbuminemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome 1 0.040 None 1.000 4 2009 2019
CUI: C0878666
Disease: Analbuminemia
Analbuminemia
phenotype Finding 1 3 0.400 None 1.000 3 3 1994 2005
CUI: C0396009
Disease: Pharyngocutaneous fistula
Pharyngocutaneous fistula
phenotype Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases Disease or Syndrome 1 0.020 None 1.000 2 2018 2020
CUI: C0009792
Disease: Consciousness Disorders
Consciousness Disorders
phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 1 0.010 None 1.000 1 2019 2019
CUI: C0019699
Disease: HIV Seropositivity
HIV Seropositivity
phenotype Infections; Immune System Diseases Laboratory or Test Result 1 0.300 None 1.000 1 2007 2007
CUI: C0030925
Disease: Peptic Ulcer Perforation
Peptic Ulcer Perforation
disease Digestive System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
Secondary malignant neoplasm of adrenal gland
disease Neoplasms; Endocrine System Diseases Neoplastic Process 1 0.010 None 1.000 1 2019 2019
CUI: C0155504
Disease: Serous labyrinthitis
Serous labyrinthitis
disease Otorhinolaryngologic Diseases Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C0267158
Disease: Reflux gastritis
Reflux gastritis
disease Digestive System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
Ketoacidosis due to acute alcohol intoxication
disease Nutritional and Metabolic Diseases; Chemically-Induced Disorders; Mental Disorders Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C0277977
Disease: Murphy's sign
Murphy's sign
phenotype Sign or Symptom 1 0.010 None 1.000 1 2017 2017
CUI: C0401013
Disease: Fungal peritonitis
Fungal peritonitis
disease Infections Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C0410648
Disease: Spinal instability
Spinal instability
disease Musculoskeletal Diseases Disease or Syndrome 1 0.010 None 1.000 1 2019 2019
CUI: C0860549
Disease: Refeeding Syndrome
Refeeding Syndrome
disease Nutritional and Metabolic Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C0936251
Disease: Polyradiculitis
Polyradiculitis
disease Nervous System Diseases Disease or Syndrome 1 0.010 None 1.000 1 1993 1993
CUI: C1290398
Disease: Cerebral arterial aneurysm
Cerebral arterial aneurysm
disease Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C1719910
Disease: Pressure ulcer stage 4 (disorder)
Pressure ulcer stage 4 (disorder)
disease Skin and Connective Tissue Diseases Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C1863119
Disease: Dysalbuminemic Hyperthyroxinemia
Dysalbuminemic Hyperthyroxinemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases Disease or Syndrome 1 0.010 None 1.000 1 2014 2014
CUI: C1963829
Disease: Lupus enteritis
Lupus enteritis
disease Disease or Syndrome 1 0.010 None 1.000 1 2018 2018
CUI: C1963924
Disease: Oligoanuria
Oligoanuria
disease Disease or Syndrome 1 0.010 None < 0.001 1 2017 2017
CUI: C2363925
Disease: Pleuroperitoneal communication
Pleuroperitoneal communication
disease Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C4303178
Disease: Acute hemorrhagic ulcer of rectum
Acute hemorrhagic ulcer of rectum
disease Disease or Syndrome 1 0.010 None 1.000 1 2017 2017
CUI: C4721771
Disease: Nasopharyngeal cancer stage IV
Nasopharyngeal cancer stage IV
disease Neoplastic Process 1 0.010 None 1.000 1 2017 2017
CUI: C1167806
Disease: Increased alpha-globulin
Increased alpha-globulin
phenotype Finding 1 0.100 None 0
CUI: C3889611
Disease: ALBUMIN BLENHEIM PHENOTYPE
ALBUMIN BLENHEIM PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1