ATRIAL FIBRILLATION, FAMILIAL, 14; ATFB14
General Information (adopted from Orphanet):
Synonyms, Signs:
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Number of Symptoms
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5
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OrphanetNr:
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OMIM Id:
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615378
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ICD-10:
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UMLs:
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MeSH:
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MedDRA:
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Snomed:
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Prevalence, inheritance and age of onset:
Prevalence:
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No data available.
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Inheritance:
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Age of onset:
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Disease classification (adopted from Orphanet):
Parent Diseases:
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No data available.
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1
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(HPO:0000822)
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Hypertension |
rare [HPO:skoehler]
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224 / 7739
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2
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(HPO:0004757)
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Paroxysmal atrial fibrillation |
2/2 [HPO:probinson]
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16 / 7739
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3
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(HPO:0012248)
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Prolonged PR interval |
1/2 [HPO:probinson]
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6 / 7739
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4
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(HPO:0012251)
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ST segment elevation |
2/2 [HPO:probinson]
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7 / 7739
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5
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(HPO:0000006)
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Autosomal dominant inheritance |
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2518 / 7739
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ClinVar (via SNiPA)
Gene symbol |
Variation |
Clinical significance |
Reference |