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| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
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MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
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622,528 entries
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There is 0 pattern entry.
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AMYLD1
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C2751492 |
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AMYLOID CARDIOMYOPATHY
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C2751492 |
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ATTRV30M amyloidosis
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C2751492 |
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ATTRV30M-related amyloidosis
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C2751492 |
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TRANSTHYRETIN AMYLOIDOSIS
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C2751492 |
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Transthyretin Amyloidosis
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C2751492 |
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Transthyretin amyloidosis
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C2751492 |
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Familial Transthyretin Amyloidosis
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C2751492 |
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Familial Transthyretin Cardiac Amyloidosis
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C2751492 |
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Amyloidosis, Hereditary, Transthyretin-Related
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C2751492 |
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AMYLOID POLYNEUROPATHY, FAMILIAL
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C2751492 |
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Familial Amyloid Polyneuropathy Type 1(Portuguese-Swedish-Japanese type)
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C2751492 |
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Familial Amyloid Polyneuropathy Type II (Indiana/Swiss or Maryland/German type)
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C2751492 |
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Hereditary Amyloidosis, Transthyretin-Related
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C2751492 |
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Hereditary oculoleptomeningeal amyloid angiopathy
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C2751492 |
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