JSON

syndromic agammaglobulinemia

Go to external page http://purl.obolibrary.org/obo/MONDO_0016463

A agammaglobulinemia that is part of a larger syndrome. [ MONDO:patterns/syndromic ]

Synonyms: syndromic hypogammaglobulinemia syndrome associated with agammaglobulinemia syndromic agammaglobulinemia

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:1843258 (MONDO:equivalentTo)
  • NCIT:C26931 (https://orcid.org/0000-0002-6601-2165)
  • Orphanet:229720 (MONDO:equivalentTo)
  • GARD:20596 (MONDO:GARD)
  • UMLS:C5680904 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, disease_grouping, mondo_top_grouping_hematologic_disorder, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_hereditary_disease, harrisons_view_immune_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_included, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_hematologic_disorder, rare, mondo_top_grouping_immune_system_disorder, harrisons_view_member, harrisons_view_syndromic_disease, harrisons_view_hereditary_disease, mondo_top_grouping_syndromic_disease, ordo_group_of_disorders

comment

The NCIT class hypogammaglobulinemia is implicitly syndromic so we place here.

conformsTo

http://purl.obolibrary.org/obo/mondo/patterns/syndromic.yaml

exactMatch

http://identifiers.org/medgen/1843258

http://www.orpha.net/ORDO/Orphanet_229720

http://purl.obolibrary.org/obo/NCIT_C26931

http://linkedlifedata.com/resource/umls/id/C5680904

has broad synonym

hypogammaglobulinemia

id

MONDO:0016463