Experimental Factor Ontology

Last uploaded: June 18, 2024

Preferred Name	neonatal osteosclerotic dysplasia
Synonyms
ID	http://purl.obolibrary.org/obo/MONDO_0019702
database_cross_reference	SCTID:389236000 Orphanet:93443 UMLS:C1300205 GARD:19199
exactMatch	http://linkedlifedata.com/resource/umls/id/C1300205 http://identifiers.org/snomedct/389236000 http://purl.obolibrary.org/obo/Orphanet_93443
IAO_0000233	https://github.com/monarch-initiative/mondo/issues/4948
id	MONDO:0019702
in_subset	http://purl.obolibrary.org/obo/mondo/mondo-base#rare http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare http://purl.obolibrary.org/obo/mondo/mondo-base#ordo_group_of_disorders http://purl.obolibrary.org/obo/mondo/mondo-base#disease_grouping
label	neonatal osteosclerotic dysplasia
notation	MONDO:0019702
prefLabel	neonatal osteosclerotic dysplasia
subClassOf	http://purl.obolibrary.org/obo/MONDO_0018230 http://www.ebi.ac.uk/efo/EFO_0005571
excluded_subClassOf	http://purl.obolibrary.org/obo/MONDO_0019703

Delete	Subject	Author	Type	Created
No notes to display

Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/MONDO_0019702	MONDO	SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019702	DOVES	SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019702	MONDO	LOOM
http://www.limics.org/hrdo/rdfns#pat_id_12354	HRDO	LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/389236000	SNOMEDCT	LOOM
http://www.orpha.net/ORDO/Orphanet_93443	ORDO	LOOM
http://purl.obolibrary.org/obo/MONDO_0019702	DOVES	LOOM