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Hb Bart'S Hydrops Fetalis (MONDO:0015579)

Alpha thalassemia caused by variation in all four copies of the alpha hemoglobin genes (e.g., homozygous deletion encompassing HBA1 and HBA2).

Overview

Category

Ontology ID

Internal:16382

Synonyms

Alpha-thalassemia major

HBA1;HBA2 digenic quadallelic Hb Bart’s hydrops fetalis

Haemoglobin Bart's hydrops fetalis

Hb Bart’s hydrops fetalis caused by quadallelic variation in HBA1;HBA2

Hb Bart’s hydrops fetalis related to quadallelic variation in HBA1 and HBA2

Hemoglobin Bart's hydrops fetalis

alpha-thalassemia hydrops fetalis

homozygous alpha0-thalassemia

Mapped terms

GARD:0016992

ICD9:282.49

MEDGEN:543726

Orphanet:163596

SCTID:5300004

UMLS:C0272005

Child terms

Unknown children.