- OMIM ID
-
105210
- OMIM term:
- AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
- Alternative terms:
-
HEREDITARY AMYLOIDOSIS, TRANSTHYRETIN-RELATED
TRANSTHYRETIN AMYLOIDOSIS
AMYLOID POLYNEUROPATHY, FAMILIAL; FAP AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED, INCLUDED
AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED, INCLUDED
- (∗) Location:
- 18q12.1
- (†) Associated OMIM genes:
- TTR
- (‡) Associated MGI genes:
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