Combined immunodeficiency, X-linked

Summary: A form of combined immunodificiency caused by mutations in the gene for INTERLEUKIN RECEPTOR COMMON GAMMA-CHAIN. ...1,2

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Symptoms of Combined immunodeficiency, X-linked

Clinical features: Imported from Human Phenotype Ontology (HPO)

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Types of Combined immunodeficiency, X-linked

Some types of this condition may include:3 Types of Combined immunodeficiency, X-linked:

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Genetics of Combined immunodeficiency, X-linked

Modes of inheritance: X-linked recessive inheritance (HPO, OMIM, Orphanet) ...Source: GTR (NCBI/NIH)4 ...

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Causes

See also causal information:

Names and Terminology

Synonyms: IMMUNODEFICIENCY 6 ...Source: GTR (NCBI/NIH)5 ...

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References

  1. [from MeSH]
  2. Source: GTR (NCBI/NIH): ncbi.nlm.nih.gov/ gtr/ conditions/ C1706416/ 
  3. Source: NCI Thesaurus
  4. Source: GTR (NCBI/NIH): ncbi.nlm.nih.gov/ gtr/ conditions/ C1706416/ 
  5. ibid.

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