Details of Disease | DrugMAP

General Information of Disease (ID: DIS3DRZH)

Disease Name	X-linked congenital hemolytic anemia
Synonyms	hemolytic anemia, congenital, X-linked; hemolytic anemia, congenital, X-linked, X-linked recessive
Disease Hierarchy	DIS487SI: Hereditary haemolytic anemia DIS3PN9X: X-linked disease DIS3DRZH: X-linked congenital hemolytic anemia
Disease Identifiers	MONDO ID MONDO_0060455 UMLS CUI C4746970 OMIM ID 301015 MedGen ID 1648376

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
ATP11C	OTKMV2K5	Limited	Unknown	[1]
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References

1	Mice deficient in the putative phospholipid flippase ATP11C exhibit altered erythrocyte shape, anemia, and reduced erythrocyte life span. J Biol Chem. 2014 Jul 11;289(28):19531-7. doi: 10.1074/jbc.C114.570267. Epub 2014 Jun 4.