Kidney Tissue Atlas Ontology

Last uploaded: March 16, 2024

Preferred Name	rare genetic bone development disorder
Synonyms	rare genetic skeletal development disorder
ID	http://purl.obolibrary.org/obo/MONDO_0018457
database_cross_reference	Orphanet:404584 UMLS:CN227376
exactMatch	http://linkedlifedata.com/resource/umls/id/CN227376 http://www.orpha.net/ORDO/Orphanet_404584
excluded from QC check	http://purl.obolibrary.org/obo/mondo/sparql/single-child-tags.sparql
has exact synonym	rare genetic skeletal development disorder
has modifier	http://purl.obolibrary.org/obo/MONDO_0021136
id	MONDO:0018457
imported from	http://purl.obolibrary.org/obo/mondo.owl
in_subset	http://purl.oboInOwllibrary.org/oboInOwl/mondo#ordo_group_of_disorders http://purl.oboInOwllibrary.org/oboInOwl/mondo#obsoletion_candidate
label	rare genetic bone development disorder
notation	MONDO:0018457
prefLabel	rare genetic bone development disorder
see also	https://github.com/monarch-initiative/mondo/issues/254
subClassOf	http://purl.obolibrary.org/obo/MONDO_0021147

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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/MONDO_0018457	MONDO	SAME_URI
http://purl.obolibrary.org/obo/MONDO_0018457	EFO	SAME_URI
http://www.orpha.net/ORDO/Orphanet_404584	EFO	LOOM
http://www.orpha.net/ORDO/Orphanet_404584	ORDO	LOOM