Cell Line Ontology

Last uploaded: March 21, 2022
Preferred Name

hereditary coproporphyria

Synonyms

"Hereditary coproporphyria (disorder)" EXACT [SNOMEDCT_2005_07_31:7425008]

"hereditary coproporphyria porphyria" EXACT [CSP2005:1849-7674]

"Hereditary coproporphyria" EXACT [MTHICD9_2006:277.1]

"Coproporphyrinogen oxidase deficiency" EXACT [SNOMEDCT_2005_07_31:238055004]

ID

http://purl.obolibrary.org/obo/DOID_13269

alternative term

"Hereditary coproporphyria (disorder)" EXACT [SNOMEDCT_2005_07_31:7425008]

"hereditary coproporphyria porphyria" EXACT [CSP2005:1849-7674]

"Hereditary coproporphyria" EXACT [MTHICD9_2006:277.1]

"Coproporphyrinogen oxidase deficiency" EXACT [SNOMEDCT_2005_07_31:238055004]

label

hereditary coproporphyria

prefixIRI

DOID:13269

prefLabel

hereditary coproporphyria

see also

OMIM2009_05_01:121300

SNOMEDCT_2010_1_31:7425008

UMLS_CUI:C0162531

URI: http://www.ebi.ac.uk/cellline#hereditary_coproporphyria

SNOMEDCT_2010_1_31:238055004

MSH2010_2010_02_22:D046349

subClassOf

http://purl.obolibrary.org/obo/DOID_3133

http://purl.obolibrary.org/obo/DOID_331

http://purl.obolibrary.org/obo/DOID_5749

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_13269 DOID SAME_URI
http://purl.obolibrary.org/obo/DOID_13269 BAO SAME_URI
http://purl.obolibrary.org/obo/DOID_13269 HHEAR SAME_URI
http://purl.obolibrary.org/obo/DOID_13269 NIFSTD SAME_URI
http://purl.obolibrary.org/obo/DOID_13269 FNS-H SAME_URI
http://purl.obolibrary.org/obo/MONDO_0007369 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0007369 EFO LOOM
http://purl.obolibrary.org/obo/DOID_13269 DOID LOOM
http://purl.obolibrary.org/obo/DOID_13269 BAO LOOM
http://purl.obolibrary.org/obo/DOID_13269 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_13269 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_13269 FNS-H LOOM
http://purl.obolibrary.org/obo/DERMO_0000564 DERMO LOOM
http://www.owl-ontologies.com/unnamed.owl#RID14457 DERMLEX LOOM
http://nanbyodata.jp/ontology/NANDO_1200813 NANDO LOOM
http://purl.bioontology.org/ontology/MEDDRA/10019866 MEDDRA LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/7425008 SNOMEDCT LOOM
http://identifiers.org/omim/121300 REXO LOOM
http://identifiers.org/omim/121300 GEXO LOOM
http://identifiers.org/omim/121300 RETO LOOM
http://purl.obolibrary.org/obo/OMIM_121300 CCO LOOM
http://purl.obolibrary.org/obo/MONDO_0007369 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0007369 DOVES LOOM
http://www.orpha.net/ORDO/Orphanet_79273 ORDO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Hereditary_Coproporphyria CSEO LOOM
http://www.limics.org/hrdo/rdfns#pat_id_11299 HRDO LOOM
http://purl.bioontology.org/ontology/RCD/Xa01L RCD LOOM
http://nanbyodata.jp/ontology/NANDO_2201264 NANDO LOOM
http://purl.bioontology.org/ontology/SNMI/D6-88320 SNMI LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_13269 NATPRO LOOM
http://purl.obolibrary.org/obo/NCIT_C84759 BERO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84759 NCIT LOOM

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