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MIM:602079 - TRIMETHYLAMINURIA; TMAU
Xenbase Genes: fmo3
Human Disease Resource: MIM
| MONDO:0011182 - trimethylaminuria |
| MONDO:0018767 - severe primary trimethylaminuria |
| DOID:0080361 - trimethylaminuria |
|
| MONDO:0011182 - trimethylaminuria |
| MONDO:0018767 - severe primary trimethylaminuria |
| DOID:0080361 - trimethylaminuria |