SNOMED Terminos Clinicos

Last uploaded: January 31, 2024
Preferred Name

eliptocitosis hereditaria

Synonyms

eliptocitosis congénita

ovalocitosis hereditaria

eliptocitosis hereditaria (trastorno)

ID

http://purl.bioontology.org/ontology/SCTSPA/191169008

Active

1

altLabel

eliptocitosis congénita

ovalocitosis hereditaria

eliptocitosis hereditaria (trastorno)

CASE SIGNIFICANCE ID

900000000000448009

cui

C0013902

DEFINITION STATUS ID

900000000000073002

Effective time

20200131

Has associated morphology

http://purl.bioontology.org/ontology/SCTSPA/45028007

Has finding site

http://purl.bioontology.org/ontology/SCTSPA/41898006

Has interpretation

http://purl.bioontology.org/ontology/SCTSPA/281300000

http://purl.bioontology.org/ontology/SCTSPA/52101004

Has pathological process

http://purl.bioontology.org/ontology/SCTSPA/308490002

interprets

http://purl.bioontology.org/ontology/SCTSPA/14089001

http://purl.bioontology.org/ontology/SCTSPA/404227002

http://purl.bioontology.org/ontology/SCTSPA/441689006

Module ID

450829007

notation

191169008

Occurs in

http://purl.bioontology.org/ontology/SCTSPA/255399007

prefLabel

eliptocitosis hereditaria

Subset member

450828004~ACCEPTABILITYID~900000000000549004

450828004~ACCEPTABILITYID~900000000000548007

tui

T047

Type ID

900000000000003001

900000000000013009

subClassOf

http://purl.bioontology.org/ontology/SCTSPA/363070008

http://purl.bioontology.org/ontology/SCTSPA/38911009

http://purl.bioontology.org/ontology/SCTSPA/42601008

http://purl.bioontology.org/ontology/SCTSPA/234409003

http://purl.bioontology.org/ontology/SCTSPA/276654001

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