ALB, albumin, 213

N. diseases: 1198; N. variants: 21
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0342185
Disease: Hyperthyroxinemia, Familial Dysalbuminemic
Hyperthyroxinemia, Familial Dysalbuminemic 		0.800 GeneticVariation disease CLINVAR
CUI: C0239981
Disease: Hypoalbuminemia
Hypoalbuminemia 		0.500 Biomarker disease HPO
CUI: C0020649
Disease: Hypotension
Hypotension 		0.400 Biomarker phenotype HPO
CUI: C0020639
Disease: Hypoproteinemia
Hypoproteinemia 		0.340 Biomarker disease HPO
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia 		0.330 Biomarker disease HPO
CUI: C0028754
Disease: Obesity
Obesity 		0.200 Biomarker disease HPO
CUI: C0015672
Disease: Fatigue
Fatigue 		0.160 Biomarker phenotype HPO
CUI: C0020443
Disease: Hypercholesterolemia
Hypercholesterolemia 		0.150 Biomarker disease HPO
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0.130 Biomarker disease HPO
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion 		0.100 Biomarker phenotype HPO
CUI: C0023787
Disease: Lipodystrophy
Lipodystrophy 		0.100 Biomarker disease HPO
CUI: C0079924
Disease: Oligohydramnios
Oligohydramnios 		0.100 Biomarker phenotype HPO
CUI: C0151526
Disease: Premature Birth
Premature Birth 		0.100 Biomarker phenotype HPO
CUI: C0151669
Disease: Increased antibody level in blood
Increased antibody level in blood 		0.100 Biomarker phenotype HPO
CUI: C0235991
Disease: Small for gestational age (disorder)
Small for gestational age (disorder) 		0.100 Biomarker phenotype HPO
CUI: C0302511
Disease: Small for gestational age fetus
Small for gestational age fetus 		0.100 Biomarker phenotype HPO
CUI: C0542571
Disease: Facial edema
Facial edema 		0.100 Biomarker disease HPO
CUI: C0574002
Disease: Edema of foot (finding)
Edema of foot (finding) 		0.100 Biomarker phenotype HPO
CUI: C1167806
Disease: Increased alpha-globulin
Increased alpha-globulin 		0.100 Biomarker phenotype HPO
CUI: C3163798
Disease: Recurrent lower respiratory tract infection
Recurrent lower respiratory tract infection 		0.100 Biomarker phenotype HPO
CUI: C3889611
Disease: ALBUMIN BLENHEIM PHENOTYPE
ALBUMIN BLENHEIM PHENOTYPE 		0.100 CausalMutation phenotype CLINVAR
CUI: C4012968
Disease: Mild global developmental delay
Mild global developmental delay 		0.100 Biomarker phenotype HPO
CUI: C4015752
Disease: ALBUMIN B PHENOTYPE
ALBUMIN B PHENOTYPE 		0.100 CausalMutation phenotype CLINVAR
CUI: C4015776
Disease: ANALBUMINEMIA BAGHDAD
ANALBUMINEMIA BAGHDAD 		0.100 CausalMutation phenotype CLINVAR
CUI: C4280743
Disease: Low pulse pressure
Low pulse pressure 		0.100 Biomarker phenotype HPO