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Metadata
ID DOID:0061059
Name immunodeficiency 89
Definition A primary immunodeficiency disease that is characterized by adult onset of recurrent infections, allergies, microcytic anemia, and Crohn disease and that has_material_basis_in homozygous mutation in the CARD10 gene on chromosome 22q13.
https://pubmed.ncbi.nlm.nih.gov/32238915/
Xrefs

MIM:619632
Synonyms

immunodeficiency 89 and autoimmunity [EXACT]
Parent Relationships

is_a primary immunodeficiency disease

is_a autosomal recessive disease
Subclass Logical Relationships

existence starts during some Adult onset

has material basis in some autosomal recessive inheritance

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