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Metadata
ID	DOID:0061094
Name	immunodeficiency 129
Definition	A T cell deficiency that is characterized by recurrent bacterial, viral, and fungal infections beginning in the first or second decades of life and that has_material_basis_in homozygous mutation in the RHOH gene on chromosome 4p14. https://pubmed.ncbi.nlm.nih.gov/38775840/
Xrefs	MIM:618307
Parent Relationships	is_a T cell deficiency is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance existence starts during some (Young adult onset or Pediatric onset)