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: C0000786
Disease: Spontaneous abortion
Spontaneous abortion
phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 188 0.100 None 0
CUI: C0023787
Disease: Lipodystrophy
Lipodystrophy
disease Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases Disease or Syndrome 226 28 0.100 None 0
CUI: C0079924
Disease: Oligohydramnios
Oligohydramnios
phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 129 21 0.100 None 0
CUI: C0151526
Disease: Premature Birth
Premature Birth
phenotype Female Urogenital Diseases and Pregnancy Complications Pathologic Function 192 50 0.100 None 0
CUI: C0151669
Disease: Increased antibody level in blood
Increased antibody level in blood
phenotype Finding 27 0.100 None 0
Small for gestational age (disorder)
phenotype Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications Finding 181 34 0.100 None 0
CUI: C0302511
Disease: Small for gestational age fetus
Small for gestational age fetus
phenotype Pathological Conditions, Signs and Symptoms Finding 156 0.100 None 0
CUI: C0542571
Disease: Facial edema
Facial edema
disease Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Male Urogenital Diseases; Immune System Diseases; Cardiovascular Diseases Pathologic Function 9 1 0.100 None 0
CUI: C0574002
Disease: Edema of foot (finding)
Edema of foot (finding)
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 19 0.100 None 0
CUI: C1167806
Disease: Increased alpha-globulin
Increased alpha-globulin
phenotype Finding 1 0.100 None 0
Recurrent lower respiratory tract infection
phenotype Disease or Syndrome 23 0.100 None 0
CUI: C3889611
Disease: ALBUMIN BLENHEIM PHENOTYPE
ALBUMIN BLENHEIM PHENOTYPE
phenotype Finding 1 1 0.100 None 0 1
CUI: C4012968
Disease: Mild global developmental delay
Mild global developmental delay
phenotype Finding 36 13 0.100 None 0
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
EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases Disease or Syndrome 3 16 0.100 None 0 1
CUI: C0025290
Disease: Aseptic Meningitis
Aseptic Meningitis
disease Nervous System Diseases Disease or Syndrome 17 0.300 None 1.000 3 1970 1971
CUI: C0026848
Disease: Myopathy
Myopathy
group Musculoskeletal Diseases; Nervous System Diseases Disease or Syndrome 634 166 0.300 None 1.000 1 1973 1973
CUI: C0221026
Disease: X-linked agammaglobulinemia
X-linked agammaglobulinemia
disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 68 69 0.010 None 1.000 1 1973 1973
CUI: C0234230
Disease: Pain, Burning
Pain, Burning
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 56 0.300 None 1.000 1 1973 1973
CUI: C0234238
Disease: Ache
Ache
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.300 None 1.000 1 1973 1973
CUI: C0234254
Disease: Radiating pain
Radiating pain
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 51 0.300 None 1.000 1 1973 1973
CUI: C0458257
Disease: Pain, Splitting
Pain, Splitting
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.300 None 1.000 1 1973 1973
CUI: C0458259
Disease: Pain, Crushing
Pain, Crushing
phenotype Pathological Conditions, Signs and Symptoms Sign or Symptom 50 0.300 None 1.000 1 1973 1973