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DOID:0050636 - familial visceral amyloidosis
Disease Ontology Definition:An amyloidosis that is characterized by the abnormal deposition of amyloid proteins that is located_in the visceral organs, primarily the kidneys.
Synonyms: AMYLOIDOSIS, FAMILIAL RENAL, German type amyloidosis, OSTERTAG TYPE AMYLOIDOSIS, systemic nonneuropathic amyloidosis
Xenbase Genes
:
fga,
lyz,
b2m,
apoa1
| MONDO:0007099 - hyoid neural crest |
| MIM:105200 - AMYLOIDOSIS, HEREDITARY SYSTEMIC 2; AMYLD2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
amyloidosis (is_a),
autosomal dominant disease (is_a),
inherited metabolic disorder (is_a)