immunodeficiency 36

Summary
Synonym
  • IMD36
  • activated phosphoinositide 3-kinase delta syndrome 2
Definition
A combined T cell and B cell immunodeficiency characterized by recurrent respiratory tract infections, lymphoproliferation, and antibody deficiency that has_material_basis_in heterozygous mutation in the PIK3R1 gene on chromosome 5q13.1.
Super Class
autosomal dominant disease combined T cell and B cell immunodeficiency
Disease Ontology
DOID:0111949
Mondo Disease Ontology
UMLS
NCI Thesaurus
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
18708 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
25513 Pik3r1 phosphoinositide-3-kinase regulatory subunit 1
The Human Phenotype Ontology
Displaying entries 11 - 20 of 21 in total
HPO ID HPO Term
HP:0000252 Microcephaly
HP:0004313 Decreased circulating antibody level
HP:0002090 Pneumonia
HP:0011956 Intestinal lymphoid nodular hyperplasia
HP:0000403 Recurrent otitis media
HP:0002665 Lymphoma
HP:0200117 Recurrent upper and lower respiratory tract infections
HP:0002240 Hepatomegaly
HP:0011109 Chronic sinusitis
HP:0001508 Failure to thrive
Displaying all 2 entries
Gene ID Gene Symbol Description
5293 PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
5728 PTEN phosphatase and tensin homolog

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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