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Ollier disease

Go to external page http://purl.obolibrary.org/obo/MONDO_0008145

A rare primary bone dysplasia disorder characterized by the development of multiple mainly unilateral or asymmetrically distributed enchondromas throughout the metaphyses of the long bones. [ Orphanet:296 ]

Synonyms: dyschondroplasia osteochondromatosis Ollier type enchondromatosis enchondromatosis, multiple Kast's syndrome enchondromatosis with haemangiomata Ollier's disease Ollier disease

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C3008 (MONDO:equivalentTo)
  • MEDGEN:41775 (MONDO:equivalentTo)
  • NORD:1526 (MONDO:NORD)
  • GARD:7251 (MONDO:GARD)
  • SCTID:46041001 (MONDO:directSiblingOf)
  • MedDRA:10014642 (Orphanet:296/e)
  • NANDO:2200049 (https://orcid.org/0000-0003-0011-764X)
  • OMIM:166000 (Orphanet:296/e)
  • NCIT:C3213 (MONDO:directSiblingOf)
  • UMLS:C0014084 (MONDO:equivalentTo)
  • SCTID:268274005 (MONDO:equivalentTo)
  • DOID:4624 (MONDO:equivalentTo)
  • NANDO:2201015 (https://orcid.org/0000-0003-0011-764X)
  • Orphanet:296 (OMIM:166000)
Subsets

gard_rare, ordo_disorder, matrix_llm__is_cancer_other, harrisons_view_connective_tissue_disorder, matrix_txgnn_grouping_cancer_or_benign_tumor, matrix_llm__txgnn_other, mondo_top_grouping_member, nord_rare, matrix_included, mondo_top_grouping_cancer_or_benign_tumor, matrix_txgnn_grouping_member, rare, harrisons_view_musculoskeletal_system_disorder, orphanet_rare, matrix_llm__is_glucose_dysfunction_other, otar, 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_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_cancer_or_benign_tumor, harrisons_view_member, harrisons_view_hereditary_disease, mondo_top_grouping_connective_tissue_disorder

closeMatch

http://identifiers.org/meddra/10014642

exactMatch

http://purl.obolibrary.org/obo/DOID_4624

http://identifiers.org/medgen/41775

http://identifiers.org/snomedct/268274005

http://purl.obolibrary.org/obo/NCIT_C3008

http://linkedlifedata.com/resource/umls/id/C0014084

https://omim.org/entry/166000

http://www.orpha.net/ORDO/Orphanet_296

excluded subClassOf

http://purl.obolibrary.org/obo/MONDO_0019716

http://purl.obolibrary.org/obo/MONDO_0019708

http://purl.obolibrary.org/obo/MONDO_0015356

http://purl.obolibrary.org/obo/MONDO_0019755

http://purl.obolibrary.org/obo/MONDO_0021147

has related synonym

enchondromatosis

multiple enchondromatosis

enchondromatosis, multiple, Ollier type

multiple cartilaginous enchondroses

id

MONDO:0008145

seeAlso

https://rarediseases.info.nih.gov/diseases/7251/ollier-disease

term tracker item

https://github.com/monarch-initiative/mondo/issues/4948