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loading...| Preferred Name | Hemoglobin D disease | |
| Synonyms |
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| Definitions |
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). |
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| ID |
http://www.orpha.net/ORDO/Orphanet_90039 |
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| 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). |
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| definition_citation |
Orphanet |
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| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=90039 |
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| has_age_of_onset |
Childhood |
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| hasDbXref |
MedDRA:10055019 ICD-10:D58.2 UMLS:C0272080 ICD-11:3A51.6 |
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| label |
Hemoglobin D disease |
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| notation |
ORPHA:90039 |
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| part_of | ||
| prefixIRI |
ORDO:Orphanet_90039 |
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| prefLabel |
Hemoglobin D disease |
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| present_in |
Worldwide AND has_point_prevalence_range : Unknown |
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| treeView | ||
| subClassOf |
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