Human Phenotype Ontology

Last uploaded: January 16, 2025

Preferred Name	Chorioretinal dystrophy
Synonyms
ID	http://purl.obolibrary.org/obo/HP_0001135
database_cross_reference	UMLS:C1857627
has_alternative_id	HP:0007920 HP:0007712
has_obo_namespace	human_phenotype
id	HP:0001135
label	Chorioretinal dystrophy
notation	HP:0001135
prefLabel	Chorioretinal dystrophy
treeView	http://purl.obolibrary.org/obo/HP_0000532 http://purl.obolibrary.org/obo/HP_0000556
subClassOf	http://purl.obolibrary.org/obo/HP_0000532 http://purl.obolibrary.org/obo/HP_0000556

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/HP_0001135	UPHENO	SAME_URI
http://purl.obolibrary.org/obo/HP_0001135	OBA	SAME_URI
http://www.semanticweb.org/hamide/ontologies/2019/3/IRD_8	HAMIDEHSGH	LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU013755	OMIM	LOOM
http://www.phoc.org.cn/pmo/class/PMO_00006718	PMAPP-PMO	LOOM
rgo:23294	GAMUTS	LOOM
https://github.com/sap218/ocimido/blob/master/ontology/ocimido.owl#OCIMIDO_00431	OCIMIDO	LOOM
http://purl.obolibrary.org/obo/HP_0001135	UPHENO	LOOM
http://purl.obolibrary.org/obo/HP_0001135	OBA	LOOM
http://www.gamuts.net/entity#chorioretinal_dystrophy	GAMUTS	REST