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SNOMED CT
Last uploaded:
January 16, 2025
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| Id | http://purl.bioontology.org/ontology/SNOMEDCT/95486002
http://purl.bioontology.org/ontology/SNOMEDCT/95486002
|
|---|---|
| Preferred Name | Congenital blindness |
| Synonyms |
Congenital blindness (disorder)
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel | Congenital blindness (disorder)
|
|---|---|
| prefLabel | Congenital blindness
|
| Type ID |
900000000000003001
900000000000013009
|
| CASE SIGNIFICANCE ID | 900000000000448009
|
| notation | 95486002
|
| Effective time | 20020131
|
| Active | 1
|
| Has finding site | |
| Has pathological process | |
| subClassOf | |
| Semantic type UMLS property | |
| type | |
| Subset member | 6011000124106~MAPTARGET~G31.9
447562003~MAPRULE~TRUE
900000000000497000~MAPTARGET~XUOUE
6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA
6011000124106~MAPTARGET~
6011000124106~MAPCATEGORYID~447638001
6011000124106~MAPGROUP~1
6011000124106~MAPGROUP~2
6011000124106~MAPTARGET~H54.7
447562003~MAPGROUP~1
447562003~CORRELATIONID~447561005
6011000124106~MAPCATEGORYID~447637006
900000000000509007~ACCEPTABILITYID~900000000000548007
900000000000508004~ACCEPTABILITYID~900000000000548007
447562003~MAPADVICE~ALWAYS H54.0
447562003~MAPPRIORITY~1
447562003~MAPCATEGORYID~447637006
6011000124106~MAPRULE~IFA 720010009 | Microphthalmia with brain atrophy syndrome |
6011000124106~MAPRULE~OTHERWISE TRUE
447562003~MAPTARGET~H54.0
6011000124106~MAPADVICE~IF MICROPHTHALMIA WITH BRAIN ATROPHY SYNDROME CHOOSE G31.9 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPCATEGORYID~447639009
6011000124106~MAPADVICE~IF MICROPHTHALMIA WITH BRAIN ATROPHY SYNDROME CHOOSE Q11.2 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT
6011000124106~MAPPRIORITY~1
6011000124106~CORRELATIONID~447561005
6011000124106~MAPRULE~TRUE
6011000124106~MAPTARGET~Q11.2
6011000124106~MAPADVICE~ALWAYS H54.7 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | THIS IS A MANIFESTATION CODE FOR USE IN A SECONDARY POSITION
6011000124106~MAPPRIORITY~2
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|
| DEFINITION STATUS ID | 900000000000074008
|
| tui | T019
|
| CTV3ID | XUOUE
|
| Occurs in | |
| cui | C0005754
|
| Has associated morphology |
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