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SNOMED CT

Last uploaded: January 16, 2025
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Id http://purl.bioontology.org/ontology/SNOMEDCT/7731005
http://purl.bioontology.org/ontology/SNOMEDCT/7731005
Preferred Name

Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
Synonyms
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)
Anhidrotic ectodermal dysplasia
Hypohidrotic ectodermal dysplasia syndrome
Rapp-Hodgkin type of ectodermal dysplasia
Anhidrotic ectodermal dysplasia syndrome
Rapp-Hodgkin ectodermal dysplasia syndrome
Type http://www.w3.org/2002/07/owl#Class

All Properties

altLabel
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)
Anhidrotic ectodermal dysplasia
Hypohidrotic ectodermal dysplasia syndrome
Rapp-Hodgkin type of ectodermal dysplasia
Anhidrotic ectodermal dysplasia syndrome
Rapp-Hodgkin ectodermal dysplasia syndrome
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prefLabel
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
Type ID
900000000000003001
900000000000013009
CASE SIGNIFICANCE ID
900000000000448009
900000000000017005
notation
7731005
Effective time
20020131
Active
1
Has finding site
INACTIVATION INDICATOR
723278000
interprets
Has pathological process
subClassOf
Semantic type UMLS property
Has interpretation
type
Subset member
447562003~MAPRULE~TRUE
900000000000531004~TARGETCOMPONENT~239006001
900000000000497000~MAPTARGET~X50H8
6011000124106~MAPGROUP~1
6011000124106~MAPADVICE~ALWAYS Q82.4
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPTARGET~Q82.4
447562003~MAPTARGET~Q82.4
6011000124106~MAPPRIORITY~1
900000000000490003~VALUEID~723278000
6011000124106~CORRELATIONID~447561005
447562003~MAPADVICE~ALWAYS Q82.4
6011000124106~MAPRULE~TRUE
900000000000509007~ACCEPTABILITYID~900000000000549004
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DEFINITION STATUS ID
900000000000074008
tui
T047
T019
CTV3ID
X50H8
Occurs in
cui
C1706004
C1785148
C0162359
C0265331
Has associated morphology
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