loading...| Preferred Name |
Hyperexplexia |
|
| Synonyms |
Startle syndrome Hyperexplexia (finding) |
|
| ID |
http://purl.bioontology.org/ontology/SNOMEDCT/19557000 |
|
| Active |
1 |
|
| altLabel |
Startle syndrome Hyperekplexia Hyperexplexia (finding) |
|
| CASE SIGNIFICANCE ID |
900000000000448009 |
|
| CTV3ID |
X004z |
|
| cui |
C0234166 |
|
| DEFINITION STATUS ID |
900000000000074008 |
|
| Effective time |
20020131 |
|
| Has finding site | ||
| Has interpretation | ||
| interprets | ||
| notation |
19557000 |
|
| prefLabel |
Hyperexplexia |
|
| Subset member |
6011000124106~MAPADVICE~IF HYPEREKPLEXIA EPILEPSY SYNDROME CHOOSE Q89.8 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPADVICE~ALWAYS G25.8 | POSSIBLE REQUIREMENT FOR AN EXTERNAL CAUSE CODE 447562003~MAPRULE~TRUE 6011000124106~MAPTARGET~G40.909 6011000124106~MAPADVICE~IF HEREDITARY HYPEREKPLEXIA CHOOSE Q89.8 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~4 6011000124106~MAPADVICE~MAP SOURCE CONCEPT CANNOT BE CLASSIFIED WITH AVAILABLE DATA 6011000124106~MAPTARGET~ 6011000124106~MAPCATEGORYID~447638001 900000000000497000~MAPTARGET~X004z 447562003~MAPTARGET~G25.8 6011000124106~MAPGROUP~1 6011000124106~MAPGROUP~2 6011000124106~MAPADVICE~ALWAYS G25.3 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE 900000000000508004~ACCEPTABILITYID~900000000000549004 447562003~MAPGROUP~1 447562003~CORRELATIONID~447561005 6011000124106~MAPTARGET~Q89.8 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 900000000000508004~ACCEPTABILITYID~900000000000548007 6011000124106~MAPADVICE~IF SPORADIC HYPEREKPLEXIA CHOOSE G25.3 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 6011000124106~MAPRULE~OTHERWISE TRUE 6011000124106~MAPCATEGORYID~447639009 6011000124106~MAPRULE~IFA 724351008 | Hereditary hyperekplexia | 6011000124106~MAPADVICE~IF HYPEREKPLEXIA EPILEPSY SYNDROME CHOOSE G40.909 | MAP OF SOURCE CONCEPT IS CONTEXT DEPENDENT 6011000124106~MAPPRIORITY~1 6011000124106~MAPADVICE~ALWAYS Q89.8 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE 6011000124106~CORRELATIONID~447561005 6011000124106~MAPTARGET~G25.3 6011000124106~MAPRULE~IFA 785726009 | Hyperekplexia epilepsy syndrome | 6011000124106~MAPRULE~TRUE 6011000124106~MAPPRIORITY~3 900000000000509007~ACCEPTABILITYID~900000000000549004 6011000124106~MAPPRIORITY~2 6011000124106~MAPRULE~IFA 783705006 | Sporadic hyperekplexia | |
|
| tui |
T184 |
|
| Type ID |
900000000000003001 900000000000013009 |
|
| subClassOf |