SNOMED CT, US Edition

Last uploaded: March 22, 2026
Id http://purl.bioontology.org/ontology/SNOMEDCT/70348004
http://purl.bioontology.org/ontology/SNOMEDCT/70348004
Preferred Name

Pendred's syndrome
Synonyms
Goitre-deafness syndrome
Pendred's syndrome (disorder)
GDTH IIB
Genetic defect in thyroid hormonogenesis II B
Thyroid hormone organification defect II B
Hypothyroidism with sensorineural deafness
Pendred syndrome
Goiter-deafness syndrome
Type http://www.w3.org/2002/07/owl#Class

All Properties

prefLabel
Pendred's syndrome
altLabel
Goitre-deafness syndrome
Pendred's syndrome (disorder)
GDTH IIB
Genetic defect in thyroid hormonogenesis II B
Thyroid hormone organification defect II B
Hypothyroidism with sensorineural deafness
Pendred syndrome
Goiter-deafness syndrome
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Type ID
900000000000003001
900000000000013009
Semantic type UMLS property
Has finding site
interprets
Effective time
20020131
cui
C0271829
Has pathological process
CTV3ID
C030.
DEFINITION STATUS ID
900000000000074008
CASE SIGNIFICANCE ID
900000000000020002
900000000000448009
900000000000017005
Occurs in
tui
T047
Active
1
Has associated morphology
notation
70348004
type
subClassOf
Subset member
447562003~MAPRULE~TRUE
6011000124106~MAPGROUP~1
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
900000000000497000~MAPTARGET~C030.
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
447562003~MAPADVICE~ALWAYS E07.1 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPPRIORITY~1
6011000124106~MAPADVICE~ALWAYS E07.1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPTARGET~E07.1
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
447562003~MAPTARGET~E07.1
6011000124106~MAPRULE~TRUE
900000000000509007~ACCEPTABILITYID~900000000000549004
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