has material basis in germline mutation in ADA severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency https://github.com/monarch-initiative/mondo/issues/4200 https://github.com/monarch-initiative/mondo/issues/4521 https://rarediseases.info.nih.gov/diseases/5748/adenosine-deaminase-deficiency https://www.malacards.org/card/adenosine_deaminase_deficiency https://www.malacards.org/card/severe_combined_immunodeficiency_autosomal_recessive_t_cell_negative_b_cell_negative_nk_cell_negative_due_to_adenosine_deaminase_deficiency severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency ADA-SCID DOID:5810 ADA deficiency CSP:1560-6660 GARD:0005748 adenosine deaminase deficiency, partial, Autosomal recessive, Somatic mosaicism UMLS:C0392607 Orphanet:277 NANDO:2200696 NCIT:C3962 SCID due to ADA deficiency, early-onset A form of SCID characterized by profound lymphopenia and very low immunoglobulin levels of all isotypes resulting in severe and recurrent opportunistic infections. adenosine deaminase deficient severe combined immunodeficiency SCID due to ADA deficiency MESH:C531816 severe combined immunodeficiency due to ADA deficiency adenosine deaminase deficiency NANDO:1200323 ICD9:277.2 MedDRA:10066367 severe combined immunodeficiency due to adenosine deaminase deficiency MEDGEN:95935 OMIM:102700 SCID due to adenosine deaminase deficiency SCTID:44940001 severe combined immunodeficiency due to ADA deficiency, Autosomal recessive, Somatic mosaicism MONDO:0007064 T-B- severe combined immunodeficiency inborn disorder of purine metabolism familial severe combined immunodeficiency