PomBase home

Disease association ontology term - MONDO:0003664 - hemolytic anemia

Term summary

ID
MONDO:0003664
Name
hemolytic anemia
Ontology or CV name
Disease association
Definition
Anemia resulting from the premature destruction of the peripheral blood red cells. It may be congenital or it may be caused by infections, medications, or malignancies.

Parents

Annotation

Disease association

MONDO:0003664 - hemolytic anemia

References:

Genes:

MONDO:0010480 - anemia, nonspherocytic hemolytic, due to G6PD deficiency

References:

Genes:

MONDO:0009134 - congenital dyserythropoietic anemia type 2

References:

Genes:

MONDO:0007109 - congenital dyserythropoietic anemia type 3

References:

Genes:

MONDO:0006506 - congenital nonspherocytic hemolytic anemia

References:

Genes:

MONDO:0008494 - cryohydrocytosis

References:

Genes:

MONDO:0009902 - cutaneous porphyria

References:

Genes:

MONDO:0012204 - familial pseudohyperkalemia

References:

Genes:

MONDO:0009259 - gamma-glutamylcysteine synthetase deficiency

References:

Genes:

MONDO:0009284 - glutathione synthetase deficiency without 5-oxoprolinuria

References:

Genes:

MONDO:0009295 - glycogen storage disease VII

References:

Genes:

MONDO:0009113 - hemolytic anemia due to diphosphoglycerate mutase deficiency

References:

Genes:

MONDO:0013275 - hemolytic anemia due to glucophosphate isomerase deficiency

References:

Genes:

MONDO:0019531 - hemolytic anemia due to glutathione reductase deficiency

References:

Genes:

MONDO:0859172 - hemolytic disease of fetus and newborn, RH-induced

References:

Genes:

MONDO:0012981 - hereditary spherocytosis type 4

References:

Genes:

MONDO:0009340 - non-spherocytic hemolytic anemia due to hexokinase deficiency

References:

Genes:

MONDO:0008493 - overhydrated hereditary stomatocytosis

References:

Genes:

MONDO:0012992 - pancreatic insufficiency-anemia-hyperostosis syndrome

References:

Genes:

MONDO:0010438 - paroxysmal nocturnal hemoglobinuria 1

References:

Genes:

MONDO:0014166 - paroxysmal nocturnal hemoglobinuria 2

References:

Genes:

MONDO:0009950 - pyruvate kinase deficiency of red cells

References:

Genes:

MONDO:0012700 - renal tubular acidosis, distal, 4, with hemolytic anemia

References:

Genes:

MONDO:0019107 - Rh deficiency syndrome

References:

Genes:

MONDO:0008165 - southeast Asian ovalocytosis

References:

Genes:

MONDO:0014221 - triosephosphate isomerase deficiency

References:

Genes: