Orphanet Rare Disease Ontology

Last uploaded: July 3, 2024
Preferred Name

Genetic central nervous system and retinal vascular disease
Synonyms
ID

http://www.orpha.net/ORDO/Orphanet_183503

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?Lng=en&Expert=183503

hasDbXref

UMLS:C5681839

label

Genetic central nervous system and retinal vascular disease

notation

ORPHA:183503

Category

prefixIRI

ORDO:Orphanet_183503

prefLabel

Genetic central nervous system and retinal vascular disease

subClassOf

http://www.orpha.net/ORDO/Orphanet_557492

http://www.orpha.net/ORDO/Orphanet_71859

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