SNOMED CT, US Edition

Last uploaded: March 22, 2026
Id http://purl.bioontology.org/ontology/SNOMEDCT/193225000
http://purl.bioontology.org/ontology/SNOMEDCT/193225000
Preferred Name

Hereditary progressive muscular dystrophy
Synonyms
Hereditary progressive muscular dystrophy (disorder)
Type http://www.w3.org/2002/07/owl#Class

All Properties

prefLabel
Hereditary progressive muscular dystrophy
altLabel
Hereditary progressive muscular dystrophy (disorder)
Has clinical course
Type ID
900000000000003001
900000000000013009
Semantic type UMLS property
Has finding site
Effective time
20190731
cui
C4551827
Has pathological process
CTV3ID
F391.
DEFINITION STATUS ID
900000000000073002
CASE SIGNIFICANCE ID
900000000000448009
tui
T047
Active
1
Has associated morphology
notation
193225000
type
subClassOf
Subset member
6011000124106~MAPADVICE~ALWAYS G71.0
447562003~MAPRULE~TRUE
6011000124106~MAPTARGET~G71.09
447562003~MAPADVICE~ALWAYS G71.0
6011000124106~MAPRULE~IFA 718572004 | Bethlem myopathy |
6011000124106~MAPGROUP~1
6011000124106~MAPADVICE~IF BETHLEM MYOPATHY CHOOSE G71.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
447562003~MAPGROUP~1
900000000000497000~MAPTARGET~F391.
447562003~CORRELATIONID~447561005
6011000124106~MAPTARGET~G71.0
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~ALWAYS G71.09 | DESCENDANTS NOT EXHAUSTIVELY MAPPED
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPRULE~OTHERWISE TRUE
6011000124106~MAPRULE~IFA 718572004 | Bethlem myopathy (disorder) |
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPTARGET~G71.2
6011000124106~MAPRULE~TRUE
6011000124106~MAPADVICE~ALWAYS G71.09
6011000124106~MAPPRIORITY~2
447562003~MAPTARGET~G71.0
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