Human Health Exposure Analysis Resource

Last uploaded: July 19, 2024
Preferred Name

Duchenne muscular dystrophy
Synonyms

Muscular dystrophy, Duchenne

Definitions

A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy. OMIM mapping confirmed by DO. [SN].

ID

http://purl.obolibrary.org/obo/DOID_11723

comment

OMIM mapping confirmed by DO. [SN].

alternative label

Muscular dystrophy, Duchenne

database_cross_reference

MESH:D020388

UMLS_CUI:C0013264

SNOMEDCT_US_2023_03_01:155095006

GARD:6291

MIM:310200

NCI:C75482

definition

A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy.

OMIM mapping confirmed by DO. [SN].

has exact synonym

Muscular dystrophy, Duchenne

has material basis in

http://purl.obolibrary.org/obo/GENO_0000149

has symptom

http://purl.obolibrary.org/obo/SYMP_0000094

http://purl.obolibrary.org/obo/SYMP_0000363

has_obo_namespace

disease_ontology

id

DOID:11723

in_subset

http://purl.obolibrary.org/obo/doid#NCIthesaurus

http://purl.obolibrary.org/obo/doid#DO_rare_slim

http://purl.obolibrary.org/obo/doid#DO_FlyBase_slim

label

Duchenne muscular dystrophy

notation

DOID:11723

note

A muscular dystrophy that has_material_basis_in X-linked mutations in the DMD gene found on the X chromosome. It is characterized by rapidly progressing muscle weakness and muscle atrophy initially involving the lower extremities and eventually affecting the whole body. It affects males whereas females can be carriers. The symptoms start before the age of six and may appear at infancy.

OMIM mapping confirmed by DO. [SN].

preferred label

Duchenne muscular dystrophy

prefLabel

Duchenne muscular dystrophy

subClassOf

http://purl.obolibrary.org/obo/DOID_0080012

http://purl.obolibrary.org/obo/DOID_9884

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Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_11723 DOID SAME_URI
http://purl.obolibrary.org/obo/DOID_11723 DTO SAME_URI
http://purl.obolibrary.org/obo/DOID_11723 BAO SAME_URI
http://purl.obolibrary.org/obo/DOID_11723 DDSS SAME_URI
http://purl.obolibrary.org/obo/DOID_11723 NIFSTD SAME_URI
http://purl.obolibrary.org/obo/DOID_11723 FNS-H SAME_URI
http://purl.obolibrary.org/obo/MONDO_0010679 MONDO LOOM
http://purl.obolibrary.org/obo/DOID_11723 DOID 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 DDSS 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://nanbyodata.jp/ontology/NANDO_2200856 NANDO 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://www.orpha.net/ORDO/Orphanet_98896 ORDO LOOM
rgo:13183 GAMUTS LOOM
http://nanbyodata.jp/ontology/NANDO_1200488 NANDO 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 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0010679 DOVES LOOM
http://purl.obolibrary.org/obo/MONDO_0010679 EFO LOOM
http://purl.bioontology.org/ontology/RCD/F3910 RCD LOOM
http://www.co-ode.org/ontologies/galen#DuchenneMuscularDystrophy GALEN LOOM