[X] familial severe combined immunodeficiency

Go to external page http://purl.obolibrary.org/obo/MONDO_0031520


This is just here as a test because I lose it

Term information

database cross reference
  • OMIMPS:601457 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, matrix_llm__tag_qualy_lost_other, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, harrisons_view_immune_system_disorder, obsoletion_candidate, nord_rare, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, mondo_top_grouping_immune_system_disorder, rare, harrisons_view_member, harrisons_view_hereditary_disease

comment

Reason: duplicate. This will be merged with MONDO:0015974 severe combined immunodeficiency'

exactMatch

https://omim.org/phenotypicSeries/PS601457

id

MONDO:0031520

should conform to

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

term tracker item

https://github.com/monarch-initiative/mondo/issues/7461

Term relations