Alpha-Thalassemia Myelodysplasia Syndrome (ATMDS)

Alias:
Acquired Hemoglobin H Disease
Atmds
Alpha-Thalassemia Myelodysplasia Syndrome, Somatic
Alpha-Thalassemia-Myelodysplastic Syndrome
Acquired Hbh Disease
Acquired Alpha-Thalassemia with Myelodysplastic Syndrome
Thalassemia, Alpha, Myelodysplasia Syndrome, Somatic
Hemoglobin H Disease, Acquired
Hemoglobin H Disease Acquired
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Alpha-Thalassemia Myelodysplasia Syndrome, also known as acquired hemoglobin h disease, is related to hemolytic anemia and deficiency anemia. An important gene associated with Alpha-Thalassemia Myelodysplasia Syndrome is ATRX (ATRX Chromatin Remodeler), and among its related pathways/superpathways are Kleefstra syndrome and Defective Inhibition of DNA Recombination at Telomere Due to DAXX Mutations. Affiliated tissues include myeloid, and related phenotypes are fatigue and microcytic anemia
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
--
Adult
<1/1000000
16
95
3

Medical Symptom

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

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

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

References Literature

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PMID
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IF
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