Agammaglobulinemia, X-Linked (XLA)

Alias:
X-Linked Agammaglobulinemia
Bruton Type Agammaglobulinemia
Xla
Bruton-Type Agammaglobulinemia
Agammaglobulinemia, X-Linked 1
Bruton's Agammaglobulinemia
Hypogammaglobulinemia
Agammaglobulinemia
Btk-Deficiency
Agmx1
Imd1
Bruton Agammaglobulinemia Tyrosine Kinase Deficiency
Bruton's Sex-Linked Agammaglobulinemia
Agammaglobulinemia, X-Linked, Type 1
X-Linked Agammaglobulinemia Type 1
Bruton's Type Agammaglobulinemia
Congenital Agammaglobulinemia
Bruton's Agammaglobulinaemia
Immunodeficiency Type 1
Immunodeficiency 1
Bruton Disease
Btk Deficiency
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Agammaglobulinemia, X-Linked, also known as x-linked agammaglobulinemia, is related to autosomal agammaglobulinemia and agammaglobulinemia 4, autosomal recessive, and has symptoms including diarrhea An important gene associated with Agammaglobulinemia, X-Linked is BTK (Bruton Tyrosine Kinase), and among its related pathways/superpathways are Innate Immune System and Signal Transduction. The drugs Hyaluronic acid and Viscosupplements have been mentioned in the context of this disorder. Affiliated tissues include b cells and bone marrow, and related phenotypes are failure to thrive and chronic otitis media
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
XL
XLD
Child
<1/1000000
24
274
159

Medical Symptom

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

Gene & Mutation

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Score
Mutations
No data available

Related Drugs

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CAS Number
Status
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No data available

Disease Model

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

References Literature

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IF
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