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[X] familial nephrotic syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0002350

An instance of nephrotic syndrome that is caused by an inherited modification of the individual's genome. [ MONDO:patterns/hereditary ]

Synonyms: hereditary nephrotic syndrome congenital nephrotic syndrome

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C35337 (MONDO:equivalentTo)
  • icd11.foundation:1524476844 (MONDO:equivalentTo)
  • OMIMPS:256300 (https://orcid.org/0000-0002-6601-2165)
  • MEDGEN:502251 (MONDO:equivalentTo)
  • SCTID:48796009 (MONDO:equivalentTo)
  • DOID:2590 (MONDO:equivalentTo)
  • UMLS:C3501848 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, matrix_excluded, otar, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, matrix_llm__txgnn_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, harrisons_view_member, harrisons_view_urinary_system_disorder, harrisons_view_syndromic_disease, harrisons_view_hereditary_disease, mondo_top_grouping_syndromic_disease

conformsTo

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

exactMatch

http://identifiers.org/medgen/502251

http://identifiers.org/snomedct/48796009

http://linkedlifedata.com/resource/umls/id/C3501848

http://purl.obolibrary.org/obo/NCIT_C35337

http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1524476844

http://purl.obolibrary.org/obo/DOID_2590

https://omim.org/phenotypicSeries/PS256300

id

MONDO:0002350

should conform to

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