Digital medicine Outcomes Value Set (DOVeS) Ontology

Last uploaded: December 13, 2023
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Preferred Name

Becker muscular dystrophy
Synonyms

Becker's muscular dystrophy

muscular dystrophy, pseudohypertrophic progressive, Becker type

muscular dystrophy, Becker type

muscular dystrophy pseudohypertrophic progressive, Becker type

benign congenital myopathy

Becker dystrophinopathy

Becker muscular dystrophy

benign pseudohypertrophic muscular dystrophy

Becker muscular dystrophy, X-linked recessive

BMD
Definitions

Becker muscular dystrophy (BMD) is a neuromuscular disease characterized by progressive muscle wasting and weakness due to degeneration of skeletal, smooth and cardiac muscle.
ID

http://purl.obolibrary.org/obo/MONDO_0010311
altLabel

Becker's muscular dystrophy

muscular dystrophy, pseudohypertrophic progressive, Becker type

muscular dystrophy, Becker type

muscular dystrophy pseudohypertrophic progressive, Becker type

benign congenital myopathy

Becker dystrophinopathy

Becker muscular dystrophy

benign pseudohypertrophic muscular dystrophy

Becker muscular dystrophy, X-linked recessive

BMD
definition

Becker muscular dystrophy (BMD) is a neuromuscular disease characterized by progressive muscle wasting and weakness due to degeneration of skeletal, smooth and cardiac muscle.
has_exact_synonym

benign congenital myopathy

Becker dystrophinopathy

Becker muscular dystrophy

benign pseudohypertrophic muscular dystrophy

Becker muscular dystrophy, X-linked recessive

BMD
has_related_synonym

Becker's muscular dystrophy

muscular dystrophy, pseudohypertrophic progressive, Becker type

muscular dystrophy, Becker type

muscular dystrophy pseudohypertrophic progressive, Becker type
IAO_0000233

https://github.com/monarch-initiative/mondo/issues/4521
label

Becker muscular dystrophy
prefixIRI

MONDO:0010311
prefLabel

Becker muscular dystrophy
seeAlso

https://rarediseases.info.nih.gov/diseases/5900/becker-muscular-dystrophy
textual definition

Becker muscular dystrophy (BMD) is a neuromuscular disease characterized by progressive muscle wasting and weakness due to degeneration of skeletal, smooth and cardiac muscle.
subClassOf

http://purl.obolibrary.org/obo/MONDO_0010542

http://purl.obolibrary.org/obo/MONDO_0016899
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Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0010311 CCONT SAME_URI
http://purl.obolibrary.org/obo/MONDO_0010311 MONDO SAME_URI
http://purl.obolibrary.org/obo/MONDO_0010311 EFO SAME_URI
http://purl.obolibrary.org/obo/DOID_9883 DOID LOOM
http://nanbyodata.jp/ontology/NANDO_2200865 NANDO LOOM
rgo:23220 GAMUTS LOOM
http://bmi.utah.edu/ontologies/hfontology/C0917713 HFO LOOM
http://www.orpha.net/ORDO/Orphanet_98895 ORDO LOOM
http://purl.bioontology.org/ontology/RCTV2/F391800 RCTV2 LOOM
http://purl.obolibrary.org/obo/DOID_9883 BAO LOOM
http://purl.obolibrary.org/obo/DOID_9883 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_9883 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_9883 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_9883 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_9883 FNS-H LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/387732009 SNOMEDCT LOOM
http://purl.obolibrary.org/obo/MONDO_0010311 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0010311 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0010311 EFO LOOM
http://purl.obolibrary.org/obo/OMIM_300376 CCO LOOM
http://purl.bioontology.org/ontology/RCD/F3918 RCD LOOM
http://nanbyodata.jp/ontology/NANDO_1200489 NANDO LOOM
http://identifiers.org/omim/300376 REXO LOOM
http://identifiers.org/omim/300376 GEXO LOOM
http://identifiers.org/omim/300376 RETO LOOM
http://www.co-ode.org/ontologies/galen#BeckerMuscularDystrophy GALEN LOOM
http://id.nlm.nih.gov/mesh/D020388 MDM LOOM
http://www.limics.org/hrdo/rdfns#pat_id_13912 HRDO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0917713 OCHV LOOM