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General Information
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| Term |
familial visceral amyloidosis |
ID (Ontology) |
DOID:0050636 (Human Disease) |
| Definition |
An amyloidosis that is characterized by the abnormal deposition of amyloid proteins that is located_in the visceral organs, primarily the kidneys. |
| Also Known As |
"AMYLOIDOSIS, FAMILIAL RENAL" ; "German type amyloidosis" ; "OSTERTAG TYPE AMYLOIDOSIS" (for all, see Synonyms field below) |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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| Data Class | Field | Records |
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| Alleles (FBal) | HUMAN_DISEASE_INTERACTIONS | 1 | | Human Disease Models (FBhh) | DOID | 2 |
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Alleles | Genes | Human Disease Models |
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familial visceral amyloidosis | 1 | 1 | 2 | model of | familial visceral amyloidosis | 1 | -- | -- |
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Relationships