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| Term | progressive familial heart block type II | ID (Ontology) | DOID:0111075 (Human Disease) |
| Definition | A progressive familial heart block characterized by autosomal dominant inheritance of heart block that tends to develop along the lines of a sinus bradycardia with a left posterior hemiblock, presenting clinically as syncopal episodes, Stokes-Adams seizures, or sudden death when complete heart block supervenes that has_material_basis_in variation in the chromosome region 1q32. | ||
| Also Known As | "PFHB2" | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease________ heart conduction disease | |__progressive familial heart block__| progressive familial heart block type II |
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| Is a |
autosomal dominant disease progressive familial heart block |
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External Crossreferences & Linkouts
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MESH:C564202 MIM:140400 |
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