OBO ID: DOID:0081142
Term Name: agammaglobulinemia 10 Search Ontology:
Synonyms:
Definition: An agammaglobulinemia that is characterized by early-childhood onset of recurrent viral and bacterial infections affecting various organ systems, particularly the sinopulmonary system. and that has_material_basis_in heterozygous mutation in the SPI1 gene on chromosome 11p11. https://pubmed.ncbi.nlm.nih.gov/32384040/
References:
Ontology: Human Disease   ( DOID:0081142 )
Relationships
is a type of:
OTHER agammaglobulinemia 10 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SPI1 Agammaglobulinemia 10, autosomal dominant 619707
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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