JSON

familial scaphocephaly syndrome

Go to external page http://purl.obolibrary.org/obo/MONDO_0015704

This is just here as a test because I lose it

Term information

database cross reference
  • MEDGEN:797875 (MONDO:equivalentTo)
  • UMLS:C3267076 (MONDO:equivalentTo)
  • MedDRA:10072229 (Orphanet:169163/e)
  • GARD:20113 (MONDO:GARD)
  • Orphanet:169163 (MONDO:equivalentTo)
Subsets

gard_rare, matrix_llm__is_cancer_other, disease_grouping, mondo_top_grouping_member, matrix_llm__txgnn_other, matrix_included, nord_rare, rare, harrisons_view_musculoskeletal_system_disorder, mondo_top_grouping_syndromic_disease, 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, mondo_top_grouping_musculoskeletal_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_syndromic_disease, mondo_top_grouping_disorder_of_development_or_morphogenesis, harrisons_view_hereditary_disease, ordo_group_of_disorders

closeMatch

http://identifiers.org/meddra/10072229

exactMatch

http://www.orpha.net/ORDO/Orphanet_169163

http://identifiers.org/medgen/797875

http://linkedlifedata.com/resource/umls/id/C3267076

id

MONDO:0015704

term tracker item

https://github.com/monarch-initiative/mondo/issues/6751

Term relations