| Current Concept: |
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Fullyspecifiedname:
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Congenital Horner syndrome (disorder) |
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ConceptId:
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770626007 |
SNOMED Definition:
(Full definition may include Is A relationships NOT present in Subset) |
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Is a |
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Autosomal dominant hereditary disorder (disorder) |
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Is a |
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Congenital disease (disorder) |
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Is a |
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Developmental hereditary disorder (disorder) |
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Is a |
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Horner syndrome (disorder) |
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Is a |
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Inherited autonomic nervous system disorder (disorder) |
| Group 1 |
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Occurrence (attribute) |
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Congenital (qualifier value)
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Pathological process (attribute) |
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Pathological developmental process (qualifier value)
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Finding site (attribute) |
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Sympathetic nerve structure (body structure)
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This concept's defining relationships are necessary but do not sufficiently define it (a.k.a. primitive).
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| Default Descriptions (Synonyms):
Show DescriptionIDs
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Fully specified name: |
Congenital Horner syndrome (disorder) |
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Synonym: |
Sindrome di Horner - congenita |
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Synonym: |
Congenital Horner syndrome |
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Synonym: |
Congenital Claude Bernard Horner syndrome |
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AAEP Diagnosis Terms
Description Preferences: |
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Preferred:
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Congenital Horner syndrome |
