PMO Precision Medicine Ontology

Last uploaded: December 16, 2020
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Id http://www.phoc.org.cn/pmo/class/PMO_00036711
http://www.phoc.org.cn/pmo/class/PMO_00036711
Preferred Name

Muscular Dystrophies
Definitions
A myopathy is characterized by progressive skeletal muscle weakness degeneration.
Type http://www.w3.org/2002/07/owl#Class

All Properties

label
Muscular Dystrophies
prefLabel
Muscular Dystrophies
Synonym
Progressive muscular dystrophy, hereditary
Muscular Dystrophy
Hereditary progressive muscular dystrophy, NOS
muscular dystrophies
Muscular dystrophy syndrome
Dystrophies, Muscular
Heredit.progres.musc.dystrophy
Congenital progressive muscular dystrophy
Hereditary progressive muscular dystrophy (disorder)
Myodystrophicas
Muscular Dystrophies [Disease/Finding]
MD
Muscular dystrophy
muscular dystrophy
Myodystrophica
Muscular dystrophy NOS
Myodystrophies
Dystrophic Muscle Diseases and Syndromes
Hered.progres.musc.dystr. NOS
Hereditary progressive muscular dystrophy NOS (disorder)
Myodystrophy
Hereditary progressive muscular dystrophy
Progressive muscular dystrophy
PMD - Progressive muscul dystr
progressive muscular dystrophy (diagnosis)
Dystrophy (Muscular)
Muscular dystrophy (disorder)
Muscular dystrophy, NOS
Hereditary progressive muscular dystrophy NOS
MUSCULAR DYSTROPHY
Dystrophy;muscular
Hered prog musc dystrphy
PMD - Progressive muscular dystrophy
MD - Muscular dystrophy
progressive muscular dystrophy
Dystrophy, Muscular
Dystrophic muscle disease or syndrome
myodystrophy
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Definition
A myopathy is characterized by progressive skeletal muscle weakness degeneration.
PMOID
PMO:00036711
MCID
MC00008500
prefixIRI
pmo:PMO_00036711
Database_Cross_Reference
SNMI:DA-51100
RCD:F391z
MTH:NOCODE
SNOMEDCT_US:267712004
CCPSS:0046013
ICD10:G71.0
SNM:D-8020
SNOMEDCT_US:44292004
ICD10CM:G71.0
PSY:32610
MDR:10019897
COSTAR:NOCODE
PSY:15700
SNOMEDCT_US:193236007
ICPC2P:L99093
LCH:U003066
SNMI:DA-51200
ICPC2P:N99007
OMIM:MTHU037519
MDR:10028356
DO:DOID:9884
NCI:C84910
SNM:D-8021
MEDLINEPLUS:335
MSH:D009136
NDFRT:N0000002065
NCI:OMFAQ
RCD:F391.
CSP:1849-6662
MTHICD9:359.1
AOD:0000005065
MDR:10028357
MEDCIN:32350
SNM:NOCODE
SNOMEDCT_US:193257004
SNOMEDCT_US:155095006
LCH_NW:sh85088693
SNOMEDCT_US:73297009
ICD10AM:G71.0
NCI_NICHD:C84910
HPO:HP:0003560
CHV:0000008362
ICD9CM:359.1
RCD:Xa0lL
SNOMEDCT_US:193225000
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Tree Number
T9.21.13.1.9.1
T9.3.1.9.1
T9.8.4.38
subClassOf
type
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