OBO ID: DOID:0111939
Term Name: immunodeficiency 37 Search Ontology:
Synonyms:
  • IMD37
Definition: A combined T cell and B cell immunodeficiency characterized by hypogammaglobulinemia with profoundly reduced memory B cells and memory T cells and increased numbers of circulating naive lymphocytes that has_material_basis_in homozygous or compound heterozygous mutation in BCL10 on chromosome 1p22.3. https://pubmed.ncbi.nlm.nih.gov/25365219/
References:
Ontology: Human Disease   (DOID:0111939)
OTHER immunodeficiency 37 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
BCL10 ?Immunodeficiency 37 616098
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None