Disease #00103 (Amyloidosis, Hereditary, Transthyretin-Related, OMIM:105210)
Official abbreviation |
- |
Name |
Amyloidosis, Hereditary, Transthyretin-Related |
OMIM ID |
105210 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
6 |
Phenotype entries for this disease |
- |
Associated with 1 gene |
TTR |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Individuals
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