Orphanet Rare Disease Ontology

Last uploaded: December 13, 2023
Preferred Name

Duchenne muscular dystrophy

Synonyms

Severe dystrophinopathy, Duchenne type

Definitions

A rare, genetic, muscular dystrophy characterized by rapidly progressive muscle weakness and wasting due to degeneration of skeletal, smooth and cardiac muscle.

ID

http://www.orpha.net/ORDO/Orphanet_98896

alternative_term

Severe dystrophinopathy, Duchenne type

DMD

definition

A rare, genetic, muscular dystrophy characterized by rapidly progressive muscle weakness and wasting due to degeneration of skeletal, smooth and cardiac muscle.

definition_citation

Orphanet

expertlink

https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=98896

has_age_of_onset

Childhood

has_inheritance

X-linked recessive

hasDbXref

ICD-10:G71.0

MedDRA:10013801

ICD-11:8C70.1

OMIM:310200

MeSH:D020388

UMLS:C0013264

label

Duchenne muscular dystrophy

notation

ORPHA:98896

part_of

http://www.orpha.net/ORDO/Orphanet_522522

http://www.orpha.net/ORDO/Orphanet_611314

http://www.orpha.net/ORDO/Orphanet_262

http://www.orpha.net/ORDO/Orphanet_207085

http://www.orpha.net/ORDO/Orphanet_519347

prefixIRI

ORDO:Orphanet_98896

prefLabel

Duchenne muscular dystrophy

present_in

Canada AND has_birth_prevalence_average_value : 10.5 AND has_birth_prevalence_range : 1-5 / 10 000

Worldwide AND has_point_prevalence_average_value : 2.8 AND has_point_prevalence_range : 1-9 / 100 000

Japan AND has_point_prevalence_average_value : 3.56 AND has_point_prevalence_range : 1-9 / 100 000

Ireland AND has_point_prevalence_average_value : 4.26 AND has_point_prevalence_range : 1-9 / 100 000

Netherlands AND has_birth_prevalence_average_value : 12.0 AND has_birth_prevalence_range : 1-5 / 10 000

South Africa AND has_point_prevalence_average_value : 0.47 AND has_point_prevalence_range : 1-9 / 1 000 000

Ireland AND has_birth_prevalence_average_value : 8.2 AND has_birth_prevalence_range : 1-9 / 100 000

United Kingdom AND has_birth_prevalence_average_value : 9.7 AND has_birth_prevalence_range : 1-9 / 100 000

United States AND has_birth_prevalence_average_value : 14.0 AND has_birth_prevalence_range : 1-5 / 10 000

Worldwide AND has_birth_prevalence_average_value : 9.9 AND has_birth_prevalence_range : 1-9 / 100 000

United Kingdom AND has_point_prevalence_average_value : 4.14 AND has_point_prevalence_range : 1-9 / 100 000

Puerto rico AND has_point_prevalence_average_value : 2.59 AND has_point_prevalence_range : 1-9 / 100 000

Egypt AND has_lifetime_prevalence_average_value : 7.66 AND has_lifetime_prevalence_range : 1-9 / 100 000

Italy AND has_point_prevalence_average_value : 1.7 AND has_point_prevalence_range : 1-9 / 100 000

Denmark AND has_point_prevalence_average_value : 2.75 AND has_point_prevalence_range : 1-9 / 100 000

treeView

http://www.orpha.net/ORDO/Orphanet_522522

http://www.orpha.net/ORDO/Orphanet_611314

http://www.orpha.net/ORDO/Orphanet_262

http://www.orpha.net/ORDO/Orphanet_207085

http://www.orpha.net/ORDO/Orphanet_519347

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_98896 EFO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0010679 EFO LOOM
http://purl.obolibrary.org/obo/DOID_11723 DOID LOOM
http://purl.obolibrary.org/obo/MONDO_0010679 MONDO LOOM
http://purl.obolibrary.org/obo/DOID_11723 DTO LOOM
http://purl.obolibrary.org/obo/DOID_11723 BAO LOOM
http://purl.obolibrary.org/obo/DOID_11723 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_11723 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_11723 FNS-H LOOM
http://purl.bioontology.org/ontology/RCTV2/F391000 RCTV2 LOOM
http://www.ebi.ac.uk/efo/EFO_0000429 CLO LOOM
http://www.projecthalo.com/aura#Duchenne-Muscular-Dystrophy AURA LOOM
http://identifiers.org/omim/310200 REXO LOOM
http://identifiers.org/omim/310200 GEXO LOOM
http://identifiers.org/omim/310200 RETO LOOM
http://purl.obolibrary.org/obo/OMIM_310200 CCO LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_11723 NATPRO LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0013264 MEDLINEPLUS LOOM
http://purl.bioontology.org/ontology/SNMI/DA-51220 SNMI LOOM
http://purl.bioontology.org/ontology/CSP/5006-0010 CRISP LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Duchenne_Muscular_Dystrophy CSEO LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/76670001 SNOMEDCT LOOM
http://purl.obolibrary.org/obo/NCIT_C75482 BERO LOOM
http://purl.bioontology.org/ontology/MEDDRA/10013801 MEDDRA LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C75482 NCIT LOOM
http://www.limics.org/hrdo/rdfns#pat_id_13913 HRDO LOOM
http://localhost/plosthes.2017-1#8184 PLOSTHES LOOM
http://purl.obolibrary.org/obo/MONDO_0010679 DOVES LOOM
http://www.gamuts.net/entity#Duchenne_muscular_dystrophy GAMUTS LOOM
http://purl.bioontology.org/ontology/RCD/F3910 RCD LOOM
http://www.co-ode.org/ontologies/galen#DuchenneMuscularDystrophy GALEN LOOM
http://www.gamuts.net/entity#Duchenne_muscular_dystrophy GAMUTS REST