SNOMED Terminos Clinicos

Last uploaded: August 28, 2024
Preferred Name

paraplejía espástica hereditaria
Synonyms

síndrome de paraplejía espástica familiar

paraplejía espástica hereditaria (trastorno)

enfermedad de Strumpell-Lorrain

ID

http://purl.bioontology.org/ontology/SCTSPA/39912006

Active

1

altLabel

síndrome de paraplejía espástica familiar

paraplejía espástica hereditaria (trastorno)

enfermedad de Strumpell-Lorrain

CASE SIGNIFICANCE ID

900000000000448009

900000000000017005

Cause of

http://purl.bioontology.org/ontology/SCTSPA/1263536006

http://purl.bioontology.org/ontology/SCTSPA/722599008

http://purl.bioontology.org/ontology/SCTSPA/1260397000

cui

C0037773

DEFINITION STATUS ID

900000000000073002

Effective time

20200131

Has associated morphology

http://purl.bioontology.org/ontology/SCTSPA/107669003

Has clinical course

http://purl.bioontology.org/ontology/SCTSPA/255314001

Has finding site

http://purl.bioontology.org/ontology/SCTSPA/2748008

http://purl.bioontology.org/ontology/SCTSPA/32153003

http://purl.bioontology.org/ontology/SCTSPA/62175007

Has interpretation

http://purl.bioontology.org/ontology/SCTSPA/2667000

interprets

http://purl.bioontology.org/ontology/SCTSPA/255324009

http://purl.bioontology.org/ontology/SCTSPA/363847004

Module ID

450829007

notation

39912006

prefLabel

39912006

Subset member

450828004~ACCEPTABILITYID~900000000000549004

450828004~ACCEPTABILITYID~900000000000548007

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SCTSPA/434371000124108

http://purl.bioontology.org/ontology/SCTSPA/106018006

http://purl.bioontology.org/ontology/SCTSPA/192967009

http://purl.bioontology.org/ontology/SCTSPA/698292000

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