immunodeficiency 14

Summary
Synonym
  • APDS
  • IMD14
  • PASLI disease
  • activated PI3K-delta syndrome
  • senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation
Definition
A combined T cell and B cell immunodeficiency characterized by B- and T-cell abnormalities and onset of recurrent sinopulmonary and other infections in early childhood that has_material_basis_in heterozygous activating mutation in the PIK3CD gene on chromosome 1p36.22.
Super Class
autosomal dominant disease combined T cell and B cell immunodeficiency
Disease Ontology
DOID:0111936
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5293 PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
The Human Phenotype Ontology
Displaying entries 11 - 20 of 29 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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Last updated: December 9, 2024