Search Ontology:
Human Disease

agammaglobulinemia 1

Term ID
DOID:0081136
Synonyms
Definition
An agammaglobulinemia that has_material_basis_in homozygous or compound heterozygous mutation in the mu heavy-chain gene (IGHM) on chromosome 14q32. https://pubmed.ncbi.nlm.nih.gov/32384040/
References
Ontology
Human Disease   ( DOID:0081136 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models