Details of Disease

General Information of Disease (ID: DISVMFK6)

Disease Name Heinz body anemia
Synonyms Heinz body anemias; Heinz body anemias, alpha-
Disease Hierarchy
DIS803XQ: Hemolytic anemia
DISVMFK6: Heinz body anemia
Disease Identifiers
MONDO ID
MONDO_0007705
MESH ID
C563030
UMLS CUI
C0700299
OMIM ID
140700
MedGen ID
148583
HPO ID
HP:0005511

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 4 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
HBA2 TTQO71U Limited Autosomal dominant [1]
HBA2 TTQO71U Strong Biomarker [2]
HBB TTM6HK1 Strong Autosomal dominant [3]
HBB TTM6HK1 Strong Biomarker [4]
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This Disease Is Related to 2 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
HBA2 OTW2BQF4 Limited Autosomal dominant [1]
HBB OT514IKQ Strong Autosomal dominant [3]
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References

1 Hyperunstable hemoglobin Toyama [alpha 2 136(H19)Leu----Arg beta 2]: detection and identification by in vitro biosynthesis with radioactive amino acids. Hemoglobin. 1987;11(6):539-56. doi: 10.3109/03630268709027870.
2 Separation and study of corrinoid cobalt-ligand isomers by high-performance liquid chromatography.J Chromatogr. 1991 Jan 4;536(1-2):185-91. doi: 10.1016/s0021-9673(01)89248-7.
3 Hb Madrid [beta115(G17)Ala-->Pro] in a Korean family with chronic hemolytic anemia. Hemoglobin. 2000 May;24(2):133-8. doi: 10.3109/03630260009003432.
4 Significant haemoglobinopathies: guidelines for screening and diagnosis.Br J Haematol. 2010 Apr;149(1):35-49. doi: 10.1111/j.1365-2141.2009.08054.x. Epub 2010 Jan 13.