Myeloperoxidase Deficiency (MPOD)

Alias:
Mpo Deficiency
Mpod
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Myeloperoxidase Deficiency, also known as mpo deficiency, is related to chronic myelomonocytic leukemia and chronic granulomatous disease. An important gene associated with Myeloperoxidase Deficiency is MPO (Myeloperoxidase), and among its related pathways/superpathways are Calnexin/calreticulin cycle and Antigen Presentation: Folding, assembly and peptide loading of class I MHC. Affiliated tissues include monocytes and neutrophil, and related phenotypes are abnormality of the immune system and abnormality of metabolism/homeostasis
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
All ages
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5
36
24

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
Journal
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IF
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