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[X] inherited focal segmental glomerulosclerosis

Go to external page http://purl.obolibrary.org/obo/MONDO_0005363

An instance of focal segmental glomerulosclerosis that is caused by an inherited genomic modification in an individual. [ MONDO:patterns/hereditary ]

This is just here as a test because I lose it

Term information

database cross reference
  • NANDO:2200113 (https://orcid.org/0000-0003-0011-764X)
  • OMIMPS:603278 (MONDO:equivalentTo)
  • NANDO:1200722 (https://orcid.org/0000-0003-0011-764X)
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, matrix_llm__medical_specialization_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, mondo_top_grouping_urinary_system_disorder, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, harrisons_view_urinary_system_disorder, harrisons_view_hereditary_disease

exactMatch

https://omim.org/phenotypicSeries/PS603278

id

MONDO:0005363

should conform to

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