Experimental Factor Ontology

Last uploaded: August 15, 2024
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://www.orpha.net/ORDO/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#rare

http://purl.obolibrary.org/obo/mondo#gard_rare

http://purl.obolibrary.org/obo/mondo#disease_grouping

http://purl.obolibrary.org/obo/mondo#ordo_group_of_disorders

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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