Cell Line Ontology

Last uploaded: March 21, 2022
Preferred Name

hereditary spherocytosis

Synonyms

"Minkowski Chauffard syndrome" EXACT [CSP2005:0427-1870]

"Hereditary spherocytosis" EXACT [ICD9CM_2006:282.0]

"Hereditary spherocytosis (disorder)" EXACT [SNOMEDCT_2005_07_31:55995005]

"Congenital spherocytic hemolytic anemia" EXACT [MTHICD9_2006:282.0]

"ANEMIA SPHEROCYTIC" EXACT [MTH:NOCODE]

"Hereditary spherocytosis" EXACT [SNOMEDCT_2005_07_31:154795009]

ID

http://purl.obolibrary.org/obo/DOID_12971

alternative term

"Minkowski Chauffard syndrome" EXACT [CSP2005:0427-1870]

"Hereditary spherocytosis" EXACT [ICD9CM_2006:282.0]

"Hereditary spherocytosis (disorder)" EXACT [SNOMEDCT_2005_07_31:55995005]

"Congenital spherocytic hemolytic anemia" EXACT [MTHICD9_2006:282.0]

"ANEMIA SPHEROCYTIC" EXACT [MTH:NOCODE]

"Hereditary spherocytosis" EXACT [SNOMEDCT_2005_07_31:154795009]

label

hereditary spherocytosis

prefixIRI

DOID:12971

prefLabel

hereditary spherocytosis

see also

UMLS_CUI:C0037889

ICD9CM_2010:282.0

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

MSH2010_2010_02_22:D013103

SNOMEDCT_2010_1_31:55995005

SNOMEDCT_2010_1_31:154795009

subClassOf

http://purl.obolibrary.org/obo/DOID_589

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_12971 DOID SAME_URI
http://purl.obolibrary.org/obo/DOID_12971 BAO SAME_URI
http://purl.obolibrary.org/obo/DOID_12971 HHEAR SAME_URI
http://purl.obolibrary.org/obo/DOID_12971 NIFSTD SAME_URI
http://purl.obolibrary.org/obo/DOID_12971 MIDO SAME_URI
http://purl.obolibrary.org/obo/DOID_12971 FNS-H SAME_URI
http://purl.obolibrary.org/obo/MONDO_0019350 MONDO LOOM
http://nanbyodata.jp/ontology/NANDO_2200622 NANDO LOOM
http://purl.bioontology.org/ontology/MEDDRA/10019904 MEDDRA LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/55995005 SNOMEDCT LOOM
http://purl.bioontology.org/ontology/ICD9CM/282.0 ICD9CM LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0037889 OCHV LOOM
http://purl.bioontology.org/ontology/CSP/0427-1870 CRISP LOOM
http://purl.bioontology.org/ontology/RCD/D100. RCD LOOM
http://purl.obolibrary.org/obo/DOID_12971 DOID LOOM
http://purl.obolibrary.org/obo/DOID_12971 BAO LOOM
http://purl.obolibrary.org/obo/DOID_12971 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_12971 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_12971 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_12971 FNS-H LOOM
http://purl.bioontology.org/ontology/ICD10/D58.0 ICD10 LOOM
http://purl.bioontology.org/ontology/RCTV2/D100.00 RCTV2 LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_12971 NATPRO LOOM
http://purl.bioontology.org/ontology/ICD10CM/D58.0 ICD10CM LOOM
http://purl.bioontology.org/ontology/ICPC2P/B78006 ICPC2P LOOM
http://purl.obolibrary.org/obo/MONDO_0019350 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0019350 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0019350 DOVES LOOM
http://purl.obolibrary.org/obo/NCIT_C97074 BERO LOOM
http://www.orpha.net/ORDO/Orphanet_822 ORDO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Hereditary_Spherocytosis CSEO LOOM
http://www.gamuts.net/entity#hereditary_spherocytosis GAMUTS LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C97074 NCIT LOOM
http://www.limics.org/hrdo/rdfns#pat_id_3252 HRDO LOOM
http://www.owl-ontologies.com/unnamed.owl#RID15049 DERMLEX LOOM

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