loading...| Preferred Name |
Congenital blindness |
|
| Synonyms |
Congenital blindness (disorder) |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/95486002 |
|
| Active |
1 |
|
| altLabel |
Congenital blindness (disorder) |
|
| CASE SIGNIFICANCE ID |
900000000000448009 |
|
| CTV3ID |
XUOUE |
|
| cui |
C0005754 |
|
| DEFINITION STATUS ID |
900000000000074008 |
|
| Effective time |
20020131 |
|
| Has associated morphology | ||
| Has finding site | ||
| Has pathological process | ||
| notation |
95486002 |
|
| Occurs in | ||
| prefLabel |
Congenital blindness |
|
| Subset member |
447562003~MAPRULE~TRUE 900000000000497000~MAPTARGET~XUOUE 6011000124106~MAPGROUP~1 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 447562003~MAPTARGET~H54.0 6011000124106~MAPPRIORITY~1 6011000124106~CORRELATIONID~447561005 6011000124106~MAPRULE~TRUE 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 |
|
| tui |
T019 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |