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SNOMED CT
Last uploaded:
August 28, 2024
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Preferred Name | Familial hemiplegic migraine type 1 | |
Synonyms |
Familial hemiplegic migraine type 1 (disorder) |
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Definitions |
Migraine type caused by mutations in the CACNA1A gene. |
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ID |
http://purl.bioontology.org/ontology/SNOMEDCT/1260329005 |
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Active |
1
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altLabel |
Familial hemiplegic migraine type 1 (disorder)
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CASE SIGNIFICANCE ID |
900000000000448009
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CTV3ID |
XVKE2
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cui |
C1832884
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definition |
Migraine type caused by mutations in the CACNA1A gene.
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DEFINITION STATUS ID |
900000000000074008
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Effective time |
20230228
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Has finding site | ||
notation |
1260329005
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prefLabel |
Familial hemiplegic migraine type 1
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Subset member |
447562003~MAPRULE~TRUE 6011000124106~MAPGROUP~1 900000000000497000~MAPTARGET~XVKE2 6011000124106~MAPTARGET~G43.409 447562003~MAPGROUP~1 447562003~CORRELATIONID~447561005 6011000124106~MAPCATEGORYID~447637006 900000000000509007~ACCEPTABILITYID~900000000000548007 900000000000508004~ACCEPTABILITYID~900000000000548007 6011000124106~MAPADVICE~ALWAYS G43.409 | CONSIDER ADDITIONAL CODE TO IDENTIFY SPECIFIC CONDITION OR DISEASE 447562003~MAPPRIORITY~1 447562003~MAPCATEGORYID~447637006 447562003~MAPADVICE~ALWAYS G43.3 6011000124106~MAPPRIORITY~1 6011000124106~CORRELATIONID~447561005 447562003~MAPTARGET~G43.3 6011000124106~MAPRULE~TRUE
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tui |
T047
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Type ID |
900000000000003001 900000000000013009
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subClassOf |
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