Experimental Factor Ontology

Last uploaded: November 18, 2024
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Preferred Name

inherited vitreoretinopathy
Synonyms
ID

http://purl.obolibrary.org/obo/MONDO_0020246
database_cross_reference

Orphanet:98668

GARD:19539

HP:0007773
disease has major feature

http://purl.obolibrary.org/obo/HP_0007773
exactMatch

http://purl.obolibrary.org/obo/Orphanet_98668
IAO_0000233

https://github.com/monarch-initiative/mondo/issues/6744

https://github.com/monarch-initiative/mondo/issues/6745

https://github.com/monarch-initiative/mondo/issues/6752
id

MONDO:0020246
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

inherited vitreoretinopathy
notation

MONDO:0020246
preferred label

inherited vitreoretinopathy
prefLabel

inherited vitreoretinopathy
subClassOf

http://www.ebi.ac.uk/efo/EFO_0000508

http://www.ebi.ac.uk/efo/EFO_0003839

http://purl.obolibrary.org/obo/MONDO_0100545
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