Familial hemolytic anemia

rare

A congenital hemolytic anemia caused by defects of the erythrocyte membrane, enzyme deficiencies, or hemoglobinopathies.

Identifiers: MONDO:0003689
Part of: Hemolytic anemia Hereditary disease
Also known as: anaemia hemolytic congenital · anemia hemolytic congenital · congenital hemolytic anemia · hereditary hemolytic anemia

Subtypes

Disease	ID	Subtypes	Genes
Congenital nonspherocytic hemolytic anemia	MONDO:0006506	13
Congenital dyserythropoietic anemia	MONDO:0019403	11
Hereditary spherocytosis	MONDO:0019350	5
Rh deficiency syndrome	MONDO:0019107		RHAG
X-linked congenital hemolytic anemia	MONDO:0060455
Abetalipoproteinemia	MONDO:0008692		MTTP
Cryohydrocytosis	MONDO:0008494		SLC4A1
Cutaneous porphyria	MONDO:0009902		UROS
Dehydrated hereditary stomatocytosis 2	MONDO:0014737		KCNN4
Dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema	MONDO:0008689		PIEZO1
Elliptocytosis 1	MONDO:0012731		EPB41
Elliptocytosis 2	MONDO:0007533		SPTA1
Familial pseudohyperkalemia	MONDO:0012204		ABCB6
Glycogen storage disease VII	MONDO:0009295		PFKM
Glycogen storage disease due to aldolase A deficiency	MONDO:0012747		ALDOA
Hemolytic anemia due to diphosphoglycerate mutase deficiency	MONDO:0009113		BPGM
Hemolytic disease of fetus and newborn, RH-induced	MONDO:0859172		RHD
Hereditary cryohydrocytosis with reduced stomatin	MONDO:0012143		SLC2A1
Overhydrated hereditary stomatocytosis	MONDO:0008493		RHAG
Primary CD59 deficiency	MONDO:0012858		CD59
Renal tubular acidosis, distal, 4, with hemolytic anemia	MONDO:0012700		SLC4A1
Southeast Asian ovalocytosis	MONDO:0008165		SLC4A1
Triosephosphate isomerase deficiency	MONDO:0014221		TPI1

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