Orphanet Rare Disease Ontology

Last uploaded: December 13, 2023
Preferred Name

Gaucher disease

Synonyms

Acid beta-glucosidase deficiency

Definitions

Gaucher disease (GD) is a lysosomal storage disorder encompassing three main forms (types 1, 2 and 3), a fetal form and a variant with cardiac involvement (Gaucher disease - ophthalmoplegia - cardiovascular calcification or Gaucher-like disease).

ID

http://www.orpha.net/ORDO/Orphanet_355

alternative_term

Acid beta-glucosidase deficiency

Glucocerebrosidase deficiency

definition

Gaucher disease (GD) is a lysosomal storage disorder encompassing three main forms (types 1, 2 and 3), a fetal form and a variant with cardiac involvement (Gaucher disease - ophthalmoplegia - cardiovascular calcification or Gaucher-like disease).

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=355

has_age_of_onset

All ages

has_inheritance

Autosomal recessive

hasDbXref

MeSH:D005776

OMIM:608013

OMIM:610539

UMLS:C0017205

OMIM:230900

ICD-11:5C56.0Y

OMIM:230800

OMIM:231000

OMIM:231005

ICD-10:E75.2

MedDRA:10018048

label

Gaucher disease

notation

ORPHA:355

part_of

http://www.orpha.net/ORDO/Orphanet_79225

prefixIRI

ORDO:Orphanet_355

prefLabel

Gaucher disease

present_in

Austria AND has_birth_prevalence_average_value : 5.7 AND has_birth_prevalence_range : 1-9 / 100 000

Spain AND has_point_prevalence_average_value : 0.67 AND has_point_prevalence_range : 1-9 / 1 000 000

Netherlands AND has_birth_prevalence_average_value : 1.16 AND has_birth_prevalence_range : 1-9 / 100 000

Czech Republic AND has_birth_prevalence_average_value : 1.13 AND has_birth_prevalence_range : 1-9 / 100 000

Worldwide AND has_birth_prevalence_average_value : 1.3 AND has_birth_prevalence_range : 1-9 / 100 000

Europe AND has_point_prevalence_average_value : 1.0 AND has_point_prevalence_range : 1-9 / 100 000

France AND has_birth_prevalence_average_value : 2.0 AND has_birth_prevalence_range : 1-9 / 100 000

France AND has_annual_incidence_average_value : 2.6 AND has_annual_incidence_range : 1-9 / 100 000

Australia AND has_birth_prevalence_average_value : 1.7 AND has_birth_prevalence_range : 1-9 / 100 000

Turkey AND has_birth_prevalence_average_value : 0.45 AND has_birth_prevalence_range : 1-9 / 1 000 000

Hungary AND has_birth_prevalence_average_value : 7.5 AND has_birth_prevalence_range : 1-9 / 100 000

France AND has_point_prevalence_average_value : 0.74 AND has_point_prevalence_range : 1-9 / 1 000 000

Portugal AND has_birth_prevalence_average_value : 1.35 AND has_birth_prevalence_range : 1-9 / 100 000

Europe AND has_annual_incidence_average_value : 1.7 AND has_annual_incidence_range : 1-9 / 100 000

China AND has_point_prevalence_average_value : 0.224 AND has_point_prevalence_range : 1-9 / 1 000 000

Sweden AND has_birth_prevalence_average_value : 2.11 AND has_birth_prevalence_range : 1-9 / 100 000

treeView

http://www.orpha.net/ORDO/Orphanet_79225

subClassOf

http://www.orpha.net/ORDO/Orphanet_377788

http://www.orpha.net/ORDO/Orphanet_557493

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Delete Mapping To Ontology Source
http://www.orpha.net/ORDO/Orphanet_355 EFO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0018150 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0018150 MONDO LOOM
http://www.owl-ontologies.com/unnamed.owl#RID18218 DERMLEX LOOM
http://www.phoc.org.cn/pmo/class/PMO_00038564 PMAPP-PMO LOOM
http://purl.obolibrary.org/obo/MONDO_0018150 DOVES LOOM
http://radlex.org/RID/RID34415 RADLEX LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.228.140.163.100.435.825.400 RH-MESH LOOM
http://purl.obolibrary.org/obo/DERMO_0000525 DERMO LOOM
http://doe-generated-ontology.com/OntoAD#C0017205 ONTOAD LOOM
http://purl.bioontology.org/ontology/LNC/MTHU036947 LOINC LOOM
http://purl.bioontology.org/ontology/LNC/LA14039-4 LOINC LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0017205 MEDLINEPLUS LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D005776 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.452.648.398.641.803.441 RH-MESH LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#5396 OCHV LOOM
http://identifiers.org/omim/230800 REXO LOOM
http://identifiers.org/omim/230800 GEXO LOOM
http://identifiers.org/omim/230800 RETO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C61268 NCIT LOOM
http://www.limics.org/hrdo/rdfns#pat_id_644 HRDO LOOM
http://purl.obolibrary.org/obo/OMIT_0006974 OMIT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.452.648.189.435.825.400 RH-MESH LOOM
http://purl.obolibrary.org/obo/OMIM_230800 CCO LOOM
http://purl.bioontology.org/ontology/MESH/D005776 MESH LOOM
http://bmi.utah.edu/ontologies/hfontology/C0017205 HFO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.452.132.100.435.825.400 RH-MESH LOOM
http://www.co-ode.org/ontologies/galen#GaucherDisease GALEN LOOM
http://www.semanticweb.org/rjyy/ontologies/2015/5/ESSO#Gaucher_Disease ESSO LOOM
http://www.semanticweb.org/rjyy/ontologies/2015/5/ESSO#Gaucher_Disease MEPO LOOM
http://www.semanticweb.org/rjyy/ontologies/2015/5/ESSO#Gaucher_Disease EPISEM LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.565.595.554.825.400 RH-MESH LOOM
http://purl.jp/bio/4/id/200906058846250543 IOBC LOOM
http://www.gamuts.net/entity#Gaucher_disease GAMUTS LOOM
http://purl.bioontology.org/ontology/ICD10CM/E75.22 ICD10CM LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.452.648.595.554.825.400 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.565.398.641.803.441 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.565.189.435.825.400 RH-MESH LOOM
http://purl.bioontology.org/ontology/LNC/LP113916-3 LOINC LOOM
http://purl.obolibrary.org/obo/NCIT_C61268 BERO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Gaucher_Disease CSEO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.452.584.687.803.441 RH-MESH LOOM
http://www.gamuts.net/entity#Gaucher_disease GAMUTS REST