SNOMED CT, US Edition

Last uploaded: March 22, 2026
Id http://purl.bioontology.org/ontology/SNOMEDCT/720850008
http://purl.bioontology.org/ontology/SNOMEDCT/720850008
Preferred Name

Choroidal atrophy and alopecia syndrome
Definitions
A rare ectodermal dysplasia syndrome, characterised by the association of choroidal atrophy (sometimes regional), together with other ectodermal dysplasia features including fine and sparse hair, absent or decreased lashes and eyebrows, and possibly mild visual loss and dysplastic/thick/grooved nails. A very rare ectodermal dysplasia syndrome with the association of choroidal atrophy (sometimes regional), together with other ectodermal dysplasia features including fine and sparse hair, absent or decreased lashes and eyebrows, and possibly mild visual loss and dysplastic/thick/grooved nails. A rare ectodermal dysplasia syndrome, characterized by the association of choroidal atrophy (sometimes regional), together with other ectodermal dysplasia features including fine and sparse hair, absent or decreased lashes and eyebrows, and possibly mild visual loss and dysplastic/thick/grooved nails.
Synonyms
Choroidal atrophy and alopecia syndrome (disorder)
Moloney syndrome
Regional choroidal atrophy and alopecia
Type http://www.w3.org/2002/07/owl#Class

All Properties

definition

A rare ectodermal dysplasia syndrome, characterised by the association of choroidal atrophy (sometimes regional), together with other ectodermal dysplasia features including fine and sparse hair, absent or decreased lashes and eyebrows, and possibly mild visual loss and dysplastic/thick/grooved nails.

A very rare ectodermal dysplasia syndrome with the association of choroidal atrophy (sometimes regional), together with other ectodermal dysplasia features including fine and sparse hair, absent or decreased lashes and eyebrows, and possibly mild visual loss and dysplastic/thick/grooved nails.

A rare ectodermal dysplasia syndrome, characterized by the association of choroidal atrophy (sometimes regional), together with other ectodermal dysplasia features including fine and sparse hair, absent or decreased lashes and eyebrows, and possibly mild visual loss and dysplastic/thick/grooved nails.
altLabel
Choroidal atrophy and alopecia syndrome (disorder)
Moloney syndrome
Regional choroidal atrophy and alopecia
prefLabel
Choroidal atrophy and alopecia syndrome
Type ID
900000000000003001
900000000000013009
CASE SIGNIFICANCE ID
900000000000448009
900000000000017005
notation
720850008
Effective time
20170131
Active
1
Has finding site
Has pathological process
subClassOf
Semantic type UMLS property
type
Subset member
447562003~MAPTARGET~H31.1
6011000124106~MAPADVICE~ALWAYS Q84.0
447562003~MAPRULE~TRUE
447562003~MAPTARGET~Q84.0
900000000000497000~MAPTARGET~XUuH4
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
447562003~MAPGROUP~2
900000000000508004~ACCEPTABILITYID~900000000000549004
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
6011000124106~MAPADVICE~ALWAYS H31.109 | CONSIDER LATERALITY SPECIFICATION
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPTARGET~Q82.8
447562003~MAPADVICE~ALWAYS Q84.0
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
447562003~MAPADVICE~ALWAYS Q82.8 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
447562003~MAPADVICE~ALWAYS H31.1
447562003~MAPADVICE~ALWAYS Q82.4 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
6011000124106~MAPTARGET~H31.109
447562003~MAPTARGET~Q82.4
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPRULE~TRUE
6011000124106~MAPTARGET~Q84.0
447562003~MAPGROUP~3
900000000000509007~ACCEPTABILITYID~900000000000549004
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DEFINITION STATUS ID
900000000000074008
tui
T047
CTV3ID
XUuH4
Occurs in
cui
C2931026
Has associated morphology
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