A broad classification of inherited disorders presenting at birth that affect both the cell-mediated and humoral aspects of the immune response. Circulating numbers of B lymphocytes, T lymphocytes and NK cells are variable but where present do not function properly. Susceptibility to infection is the primary concern. [ NCIT:C27871 ]
Synonyms: congenital combined immunodeficiency combined immunodeficiency CID
Term information
- NANDO:2100203 (https://orcid.org/0000-0003-0011-764X)
- UMLS:C2711630 (MONDO:equivalentTo)
- NCIT:C27871 (NCIT:C27871)
- GARD:19806 (MONDO:GARD)
- DOID:0111962 (MONDO:equivalentTo)
- DOID:628 (MONDO:equivalentTo)
- ICD9:279.2 (DOID:628)
- icd11.foundation:1616506198 (https://orcid.org/0000-0002-3458-4839)
- MEDGEN:751396 (MONDO:equivalentTo)
- Orphanet:101972 (MONDO:equivalentTo)
matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, disease_grouping, matrix_llm__txgnn_other, matrix_llm__medical_specialization_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, harrisons_view_immune_system_disorder, matrix_included, matrix_llm__tag_existing_treatment_other, clingen, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, mondo_top_grouping_immune_system_disorder, harrisons_view_member, harrisons_view_hereditary_disease, ordo_group_of_disorders
http://purl.obolibrary.org/obo/NCIT_C27871
http://www.orpha.net/ORDO/Orphanet_101972
http://purl.obolibrary.org/obo/DOID_628
http://linkedlifedata.com/resource/umls/id/C2711630
http://identifiers.org/medgen/751396
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1616506198
http://purl.obolibrary.org/obo/DOID_0111962
combined T cell and B cell immunodeficiency
combined T and B cell immunodeficiency