UMLS:C0002878 - FACTA Search

Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0002878 (hemolytic anemia)
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Human Gene/Protein
sterolin 2	12.0
tetratricopeptide repeat domain 14	12.0
Von Willebrand factor-cleaving protease	11.0
C20orf194	11.0
von Willebrand factor-cleaving protease	10.6
P5'N-1	10.6
FKSG76	10.5
diacylglycerol kinase epsilon	10.2
RHAG	10.2
PKLR	10.1
pyrimidine 5'-nucleotidase	10.1
Glutathione synthetase	10.1
RPK	9.9
Inosine triphosphatase	9.9
PN-I	9.9
vWF-CP	9.7
erythrocyte membrane protein band 4.1	9.7
uroporphyrinogen-III synthase	9.7
Rh50 protein	9.7
alpha-1 globin	9.7
inosine triphosphatase	9.6
ADAMTS13	9.5
RAB15	9.5
putative dipeptidase	9.5
glucose-6-phosphate dehydrogenase variant	9.5
P4.2	9.4
EPB42	9.4
SPTB	9.4
SLC4A1	9.3
SAMD14	9.2
zinc finger-like protein	9.2
eIF3-p44	9.2
FAM38A	9.2
Phosphoglycerate kinase	9.2
HUS	9.1
NHLRC2	9.0
Rh50 glycoprotein	9.0
ADAMTS-13	9.0
RH50	9.0
CFHR4	9.0

Disease
Mechanical hemolytic anemia	12.0
Autoimmune hemolytic disease	12.0
Gamma-glutamylcysteine synthetase deficiency	12.0
G6PD deficiency anemia	12.0
Gluthathione synthetase deficiency	12.0
Diarrhea-negative HUS	12.0
Aldolase A deficiency	12.0
Pyruvate kinase deficiency anaemia	12.0
gamma-Glutamyl transpeptidase deficiency	12.0
thrombosis; pregnancy	12.0
Alpha thalassemia intermedia	12.0
hemolytic anemia	12.0
Harderoporphyria	12.0
general; anemia	12.0
Adenylate kinase deficiency	12.0
Drug-induced hemolytic anemia	11.8
fragmentation hemolytic anemia	11.6
Hereditary stomatocytosis	11.6
Acute hemolytic anemia	11.5
SLEH1	11.5
5-Oxoprolinuria	11.3
Paroxysmal cold hemoglobinuria	11.2
5-Oxoprolinase deficiency	11.0
Rh deficiency syndrome	11.0
megalerythema	11.0
sperocytosis	11.0
Encephalitis and meningoencephalitis	11.0
hepatocholangitis	11.0
Drug-induced immune hemolytic anemia	11.0
drepanocytic anemia	11.0
Zieve's syndrome	11.0
stage I chronic lymphocytic leukemia	11.0
Brucella septicemia	11.0
Hemoglobin SE disease	11.0
pyruvate kinase deficiency	10.8
Hemoglobinuric nephrosis	10.7
Chronic cold agglutinin disease	10.7
Microangiopathic hemolytic anemia	10.5
Hypoproliferative anemia	10.5
Beta thalassemia intermedia	10.5

Enzyme
porphobilinogenase	8.5
inosine triphosphatase	8.5
5-oxoprolinase	7.9
glutathione synthetase	7.3
C3b inactivator	7.2
2,3-bisphosphoglycerate phosphatase	7.0
phosphoglyceromutase	6.8
glucose-6-phosphate dehydrogenase	6.7
pyruvate kinase	6.7
triose-phosphate isomerase	6.5
coproporphyrinogen oxidase	6.4
bromelin	6.3
GP-I	6.2
CFI	6.1
creatinase	6.1
histone-lysine N-methyltransferase	6.0
phosphoglycerate kinase	5.8
PRPP synthetase	5.7
phosphoglucose isomerase	5.7
2-keto-3-deoxy-6-phosphogluconate aldolase	5.6
nucleotidase	5.6
DAT	5.6
6-phosphogluconolactonase	5.6
coproporphyrinogen III oxidase	5.6
phosphoglycolate phosphatase	5.5
adenylate kinase	5.4
uridine kinase	5.3
lecithin:cholesterol acyltransferase	5.3
CYP7B1	5.1
sulfiredoxin	5.1
endoproteinase Asp-N	4.8
diacylglycerol kinase	4.7
5'-nucleotidase	4.7
homocysteine methyltransferase	4.7
ceruloplasmin	4.6
sarcosine oxidase	4.6
hydroxypyruvate reductase	4.6
hydroxypyruvate reductase	4.4
transaldolase	4.4
uricase	4.4