| C2751492 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED |
DO |
transthyretin amyloidosis
|
0050638 |
| C2751492 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED |
EFO |
familial amyloid neuropathy
|
0004129 |
| C2751492 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED |
MONDO |
familial amyloid neuropathy
|
0007100 |
| C2751492 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED |
MSH |
Amyloidosis, Hereditary, Transthyretin-Related
|
C567782 |
| C2751492 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED |
MSH |
Hereditary Amyloidosis, Transthyretin-Related
|
C567782 |
| C2751492 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED |
OMIM |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
|
105210 |
| C2751492 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED |
OMIM |
AMYLOIDOSIS, LEPTOMENINGEAL, TRANSTHYRETIN-RELATED
|
105210 |
| C2751492 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED |
OMIM |
AMYLOID CARDIOMYOPATHY, TRANSTHYRETIN-RELATED
|
105210 |
| C2751492 |
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED |
ORDO |
ATTRV30M amyloidosis
|
85447 |