HEMOGLOBIN NYU

MedGen UID:: 855075
•Concept ID:: C3889376
•: Finding

OMIM®:

142000

Clinical features

From HPO

Anemia

MedGen UID:: 1526
•Concept ID:: C0002871
•: Disease or Syndrome

A reduction in erythrocytes volume or hemoglobin concentration.

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Imbalanced hemoglobin synthesis

MedGen UID:: 870723
•Concept ID:: C4025177
•: Finding

Normal hemoglobin synthesis is characterized by production of equal amounts of alpha and beta globins. This term refers to a deviation from this pattern and is the main characteristic of the various forms of thalassemia.

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Abnormality of blood and blood-forming tissues
- Anemia
- Imbalanced hemoglobin synthesis

Recent clinical studies

Etiology

Molecular Characterization of δ-Thalassemia in Iran.

Kordafshari A, Amirian A, Zeinali S, Valaei A, Maryami F, Karimipoor M
Hemoglobin 2016;40(1):44-7. doi: 10.3109/03630269.2015.1092982. PMID: 26754299

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Diagnosis

First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA₂-NYU in Iran.

Amirian A, Karimipoor M, Jafarinejad M, Taghavi M, Kordafshari A, Fathi Azar S, Mohammadi MS, Zeinali S
Arch Iran Med 2011 Jan;14(1):8-11. PMID: 21194254

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MedGen

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HEMOGLOBIN NYU

Clinical features

Recent clinical studies

Etiology

Diagnosis

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