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Metadata
ID DOID:0061062
Name immunodeficiency 92
Definition A primary immunodeficiency disease that is characterized by the onset of recurrent infections in infancy or early childhood and that has_material_basis_in homozygous mutation in the REL gene on chromosome 2p16.
https://pubmed.ncbi.nlm.nih.gov/34623332/
Xrefs

MIM:619652

Parent Relationships

is_a primary immunodeficiency disease

is_a autosomal recessive disease

Subclass Logical Relationships

has material basis in some autosomal recessive inheritance

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