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: C4015752
Disease: ALBUMIN B PHENOTYPE
ALBUMIN B PHENOTYPE 		phenotype Finding 1 1 0.100 None 0 1
CUI: C4015776
Disease: ANALBUMINEMIA BAGHDAD
ANALBUMINEMIA BAGHDAD 		phenotype Finding 1 1 0.100 None 0 1
CUI: C4280743
Disease: Low pulse pressure
Low pulse pressure 		phenotype Finding 1 0.100 None 0
CUI: C1855796
Disease: Hypoproteinemia, Hypercatabolic
Hypoproteinemia, Hypercatabolic 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 2 2 0.020 None 1.000 2 1990 2006
CUI: C0024710
Disease: Mange, Sarcoptic
Mange, Sarcoptic 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C0040199
Disease: Tick-borne fever
Tick-borne fever 		disease Infections Disease or Syndrome 2 0.010 None 1.000 1 2018 2018
CUI: C0086815
Disease: Plantar Ulcer
Plantar Ulcer 		disease Skin and Connective Tissue Diseases Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C0232498
Disease: Abdominal tenderness
Abdominal tenderness 		phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 2 0.010 None 1.000 1 2019 2019
CUI: C0238132
Disease: Bronchopleural Fistula
Bronchopleural Fistula 		disease Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0238434
Disease: Epidural Abscess, Spinal
Epidural Abscess, Spinal 		disease Infections; Nervous System Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0259744
Disease: dysproteinemia
dysproteinemia 		disease Hemic and Lymphatic Diseases Disease or Syndrome 2 0.010 None 1.000 1 1988 1988
CUI: C0276758
Disease: Fusariosis
Fusariosis 		disease Infections; Skin and Connective Tissue Diseases Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0334091
Disease: Biliary hamartoma
Biliary hamartoma 		disease Neoplasms Neoplastic Process 2 0.010 None 1.000 1 1998 1998
CUI: C0334286
Disease: Bile duct cystadenocarcinoma
Bile duct cystadenocarcinoma 		disease Neoplastic Process 2 0.010 None 1.000 1 1998 1998
CUI: C0342613
Disease: Danish type familial amyloid cardiomyopathy
Danish type familial amyloid cardiomyopathy 		disease Disease or Syndrome 2 2 0.010 None 1.000 1 1985 1985
CUI: C0342957
Disease: Postoperative septic shock
Postoperative septic shock 		phenotype Pathological Conditions, Signs and Symptoms; Infections Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0376527
Disease: Skull Base Neoplasms
Skull Base Neoplasms 		group Neoplasms; Musculoskeletal Diseases Neoplastic Process 2 0.010 None 1.000 1 2018 2018
CUI: C0563305
Disease: IgA myeloma
IgA myeloma 		disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Neoplastic Process 2 0.010 None 1.000 1 2018 2018
CUI: C0948153
Disease: Portal vein stenosis
Portal vein stenosis 		disease Disease or Syndrome 2 0.010 None < 0.001 1 2017 2017
CUI: C1863557
Disease: Young Simpson syndrome
Young Simpson syndrome 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases; Mental Disorders; Behavior and Behavior Mechanisms; Cardiovascular Diseases Disease or Syndrome 2 13 0.010 None 1.000 1 2019 2019
CUI: C2930845
Disease: Stenotrophomonas maltophilia bacteremia
Stenotrophomonas maltophilia bacteremia 		disease Infections Disease or Syndrome 2 0.010 None 1.000 1 2017 2017
CUI: C3888534
Disease: Gastrointestinal wall thickening
Gastrointestinal wall thickening 		phenotype Sign or Symptom 2 0.010 None 1.000 1 2018 2018
CUI: C3897124
Disease: BCLC Stage A Hepatocellular Carcinoma
BCLC Stage A Hepatocellular Carcinoma 		disease Neoplastic Process 2 0.010 None 1.000 1 2018 2018
CUI: C4087189
Disease: Locomotive syndrome
Locomotive syndrome 		disease Disease or Syndrome 2 0.010 None 1.000 1 2019 2019
CUI: C0024043
Disease: Low T3 Syndrome
Low T3 Syndrome 		disease Endocrine System Diseases Disease or Syndrome 3 0.010 None 1.000 1 2017 2017