JSON

congenital vertebral-cardiac-renal anomalies syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0020831

Synonyms: vertebral, cardiac, renal, and limb defects syndrome VCRL

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:17961 (MONDO:GARD)
  • OMIMPS:617660 (MONDO:equivalentTo)
  • Orphanet:521438 (MONDO:equivalentTo)
  • UMLS:C5680183 (MONDO:equivalentTo)
  • MEDGEN:1814457 (MONDO:equivalentTo)
Subsets

matrix_llm__is_cancer_other, ordo_disorder, gard_rare, matrix_llm__txgnn_other, mondo_top_grouping_member, nord_rare, matrix_included, matrix_txgnn_grouping_member, rare, mondo_top_grouping_cardiovascular_disorder, orphanet_rare, matrix_llm__is_glucose_dysfunction_other, otar, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__tag_qualy_lost_other, matrix_llm__medical_specialization_other, mondo_top_grouping_hereditary_disease, matrix_txgnn_grouping_cardiovascular_disorder, matrix_llm__tag_existing_treatment_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_cardiovascular_disorder, harrisons_view_member, ordo_malformation_syndrome, harrisons_view_hereditary_disease, mondo_top_grouping_disorder_of_development_or_morphogenesis

exactMatch

http://www.orpha.net/ORDO/Orphanet_521438

http://identifiers.org/medgen/1814457

http://linkedlifedata.com/resource/umls/id/C5680183

https://omim.org/phenotypicSeries/PS617660

id

MONDO:0020831

should conform to

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