SNOMED Terminos Clinicos

Last uploaded: August 28, 2024

Preferred Name	paraplejía espástica hereditaria ligada al cromosoma X
Synonyms	paraplejía espástica hereditaria ligada al cromosoma X (trastorno)
ID	http://purl.bioontology.org/ontology/SCTSPA/724775006
Active	1
altLabel	paraplejía espástica hereditaria ligada al cromosoma X (trastorno)
CASE SIGNIFICANCE ID	900000000000017005
cui	C0751605
DEFINITION STATUS ID	900000000000073002
Effective time	20220131
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	724775006
prefLabel	724775006
Subset member	450828004~ACCEPTABILITYID~900000000000548007
tui	T047
Type ID	900000000000003001 900000000000013009
subClassOf	http://purl.bioontology.org/ontology/SCTSPA/128430005 http://purl.bioontology.org/ontology/SCTSPA/39912006

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/SNOMEDCT/724775006	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/MESH/D015419	MESH	CUI
http://purl.bioontology.org/ontology/MSHFRE/D015419	MSHFRE	CUI