SNOMED CT, US Edition

Last uploaded: March 22, 2026
Id http://purl.bioontology.org/ontology/SNOMEDCT/23536000
http://purl.bioontology.org/ontology/SNOMEDCT/23536000
Preferred Name

Iodotyrosyl coupling defect
Synonyms
Genetic defect in thyroid hormonogenesis III
Thyroid hormone coupling defect
GDTH III - genetic defect in thyroid hormonogenesis III
Iodotyrosyl coupling defect (disorder)
Hypothyroidism due to coupling defect
Congenital thyroid hormone coupling defect
Type http://www.w3.org/2002/07/owl#Class

All Properties

prefLabel
Iodotyrosyl coupling defect
altLabel
Genetic defect in thyroid hormonogenesis III
Thyroid hormone coupling defect
GDTH III - genetic defect in thyroid hormonogenesis III
Iodotyrosyl coupling defect (disorder)
Hypothyroidism due to coupling defect
Congenital thyroid hormone coupling defect
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Type ID
900000000000003001
900000000000013009
Semantic type UMLS property
Has finding site
Effective time
20020131
cui
C0342194
CTV3ID
X40Hx
DEFINITION STATUS ID
900000000000074008
CASE SIGNIFICANCE ID
900000000000020002
900000000000448009
900000000000017005
Occurs in
tui
T047
Active
1
Has associated morphology
notation
23536000
INACTIVATION INDICATOR
723277005
type
subClassOf
Subset member
447562003~MAPRULE~TRUE
900000000000490003~VALUEID~723277005
6011000124106~MAPGROUP~1
447562003~MAPADVICE~ALWAYS E03.0
447562003~MAPADVICE~ALWAYS E07.1
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
900000000000508004~ACCEPTABILITYID~900000000000548007
900000000000497000~MAPTARGET~X40Hx
447562003~MAPPRIORITY~1
6011000124106~MAPADVICE~ALWAYS E07.1
447562003~MAPCATEGORYID~447637006
447562003~MAPTARGET~E03.0
6011000124106~MAPTARGET~E07.1
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
447562003~MAPTARGET~E07.1
6011000124106~MAPRULE~TRUE
900000000000509007~ACCEPTABILITYID~900000000000549004
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