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T-B- severe combined immunodeficiency

Go to external page http://purl.obolibrary.org/obo/MONDO_0017855

T-B- severe combined immunodeficiency (SCID) is a group of rare monogenic primary immunodeficiency disorders characterized by a lack of functional peripheral T and B lymphocytes, resulting in recurrent early-onset severe respiratory viral, bacterial or fungal infections, diarrhea and failure to thrive. Hypersensitivity to ionizing radiation is a characteristic feature of some of its sub-types. [ Orphanet:317419 ]

Synonyms: T-B- SCID

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:21406 (MONDO:GARD)
  • Orphanet:317419 (MONDO:equivalentTo)
  • MEDGEN:1842252 (MONDO:equivalentTo)
  • UMLS:C5679893 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, disease_grouping, matrix_llm__medical_specialization_other, mondo_top_grouping_member, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, harrisons_view_immune_system_disorder, matrix_included, nord_rare, matrix_llm__tag_existing_treatment_other, 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

exactMatch

http://identifiers.org/medgen/1842252

http://www.orpha.net/ORDO/Orphanet_317419

http://linkedlifedata.com/resource/umls/id/C5679893

id

MONDO:0017855

Term relations