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Descriptor English: Hemoglobin H
Descriptor Spanish: Hemoglobina H
Descriptor hemoglobina H
Scope note: Hemoglobina anormal compuesta de cuatro cadenas beta. Está causada por una menor síntesis de la cadena alfa. Esta anomalía da lugar a la TALASEMIA ALFA.
Descriptor Portuguese: Hemoglobina H
Descriptor French: Hémoglobine H
Tree number(s): D12.776.124.400.463.463
D12.776.422.316.762.426.463
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D006447
Scope note: An abnormal hemoglobin composed of four beta chains. It is caused by the reduced synthesis of the alpha chain. This abnormality results in ALPHA-THALASSEMIA.
Annotation: /urine: coordinate with HEMOGLOBINURIA
Allowable Qualifiers: AA analogs & derivatives
AD administration & dosage
AE adverse effects
AG agonists
AI antagonists & inhibitors
AN analysis
BI biosynthesis
CF cerebrospinal fluid
CH chemistry
CL classification
CS chemical synthesis
DE drug effects
DF deficiency
EC economics
GE genetics
HI history
IM immunology
IP isolation & purification
ME metabolism
PD pharmacology
PH physiology
PK pharmacokinetics
PO poisoning
RE radiation effects
SD supply & distribution
ST standards
TO toxicity
TU therapeutic use
UL ultrastructure
UR urine
Registry Number: 9034-79-1
CAS Type 1 Name: Hemoglobin H
Public MeSH Note: 91; was see under HEMOGLOBINS, ABNORMAL 1973-90
History Note: 91(73); was see under HEMOGLOBINS, ABNORMAL 1973-90
Entry Version: HBH
Related: alpha-Thalassemia MeSH
DeCS ID: 22194
Unique ID: D006447
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1991/01/01
Date of Entry: 1999/01/01
Revision Date: 2016/06/28
Hemoglobin H - Preferred
Concept UI M0010121
Scope note An abnormal hemoglobin composed of four beta chains. It is caused by the reduced synthesis of the alpha chain. This abnormality results in ALPHA-THALASSEMIA.
Preferred term Hemoglobin H



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