| manager |
|
| language |
- |
| license |
- |
| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
|
MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
|
622,528 entries
|
There is 0 pattern entry.
|
Hereditary oculoleptomeningeal amyloid angiopathy
|
C2751492 |
|
|
hereditary transthyretin amyloidosis
|
C2751492 |
|
|
TTR amyloid neuropathy
|
C2751492 |
|
|
Transthyretin amyloid neuropathy
|
C2751492 |
|
|
Familial amyloid polyneuropathy
|
C2751492 |
|
|
Transthyretin amyloid polyneuropathy
|
C2751492 |
|
|
Familial amyloid polyneuropathy type I
|
C2751492 |
|
|
Familial amyloid polyneuropathy, Portuguese-Swedish-Japanese type
|
C2751492 |
|
|
Amyloidosis, Hereditary, Transthyretin-Related
|
C2751492 |
|
|
Hereditary Amyloidosis, Transthyretin-Related
|
C2751492 |
|
|
Amyloidosis, hereditary systemic 1
|
C2751492 |
|
|
amyloidosis, hereditary systemic 1
|
C2751492 |
|
|
Amyloid polyneuropathy transthyretin related
|
C2751492 |
|
