Human Disease Ontology

Last uploaded: November 1, 2024

Preferred Name	hereditary retinal dystrophy
Synonyms
ID	http://purl.obolibrary.org/obo/DOID_8500
database_cross_reference	ICD10CM:H35.5 ICD9CM:362.7 UMLS_CUI:C0154860 SNOMEDCT_US_2023_03_01:41799005 NCI:C35194
has_obo_namespace	disease_ontology
id	DOID:8500
in_subset	http://purl.obolibrary.org/obo/doid#NCIthesaurus
label	hereditary retinal dystrophy
notation	DOID:8500
prefLabel	hereditary retinal dystrophy
subClassOf	http://purl.obolibrary.org/obo/DOID_8501

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.obolibrary.org/obo/DOID_8500	CLO	SAME_URI
http://purl.obolibrary.org/obo/DOID_8500	HHEAR	SAME_URI
http://purl.obolibrary.org/obo/DOID_8500	DDSS	SAME_URI
http://purl.obolibrary.org/obo/DOID_8500	NIFSTD	SAME_URI
http://purl.obolibrary.org/obo/DOID_8500	MIDO	SAME_URI
http://purl.obolibrary.org/obo/DOID_8500	FNS-H	SAME_URI
http://purl.bioontology.org/ontology/RCD/F427.	RCD	LOOM
http://purl.obolibrary.org/obo/DOID_8500	CLO	LOOM
http://purl.obolibrary.org/obo/DOID_8500	HHEAR	LOOM
http://purl.obolibrary.org/obo/DOID_8500	DDSS	LOOM
http://purl.obolibrary.org/obo/DOID_8500	NIFSTD	LOOM
http://purl.obolibrary.org/obo/DOID_8500	MIDO	LOOM
http://purl.obolibrary.org/obo/DOID_8500	FNS-H	LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/41799005	SNOMEDCT	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Hereditary_Retinal_Dystrophy	CSEO	LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_8500	NATPRO	LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C35194	NCIT	LOOM
http://purl.bioontology.org/ontology/MEDDRA/10019899	MEDDRA	LOOM
http://purl.bioontology.org/ontology/ICD10CM/H35.5	ICD10CM	LOOM
http://purl.bioontology.org/ontology/ICD10/H35.5	ICD10	LOOM
http://purl.obolibrary.org/obo/NCIT_C35194	BERO	LOOM