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Hemoglobin D disease
Disease definition
Hemoglobin D disease(HbD) is a hemoglobinopathy characterized by production of abnormal variant hemoglobin known as hemoglobin D, with no or mild clinical manifestations (splenomegaly, very mild anemia).
ORPHA:90039
Classification level: Disorder- Synonym(s): -
- Prevalence: Unknown
- Inheritance: -
- Age of onset: Childhood
- ICD-10: D58.2
- ICD-11: 3A51.6
- OMIM: -
- UMLS: C0272080
- MeSH: -
- GARD: -
- MedDRA: 10055019
A summary on this disease is available in Español (2014) Français (2014) Nederlands (2014) Italiano (2012) Deutsch (2007)
Detailed information
Guidelines
- Clinical practice guidelines
- English (2010) - Br J Haematol
- English (2015) - Eur J Hum Genet
Genetic Testing
- Guidance for genetic testing
- Français (2019, pdf) - ANPGM


Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.