Alpha-Thalassemia (A-THAL)

Alias:
Alpha Thalassemia
Alpha Thalassaemia
Alpha Plus Thalassemia
Alpha Thalassaemia Syndrome
Thalassemias, Alpha-
Thalassemia, Alpha-
Thalassemia, Alpha
Α-Thalassemia
Thalassemia
a-Thal
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Alpha-Thalassemia, also known as alpha thalassemia, is related to hemoglobin h disease and alpha thalassemia-intellectual disability syndrome type 1, and has symptoms including angina pectoris, chest pain and edema. An important gene associated with Alpha-Thalassemia is HBA2 (Hemoglobin Subunit Alpha 2), and among its related pathways/superpathways are Glucose / Energy Metabolism and Binding and Uptake of Ligands by Scavenger Receptors. The drugs Peginterferon alfa-2b and Metformin have been mentioned in the context of this disorder. Affiliated tissues include spleen and liver, and related phenotypes are microcytic anemia and abnormal hemoglobin
Related ID:
MESH:D017085
ICD11:531667506

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
All ages
1-5/10000
96
852
108

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

#
Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
No Data Found!
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