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MIM:616154 - PEROXISOMAL FATTY ACYL-CoA REDUCTASE 1 DISORDER; PFCRD
Xenbase Genes: far1
Human Disease Resource: MIM
| MONDO:0014510 - fatty acyl-CoA reductase 1 deficiency |
| DOID:0081243 - rhizomelic chondrodysplasia punctate type 4 |
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| MONDO:0014510 - fatty acyl-CoA reductase 1 deficiency |
| DOID:0081243 - rhizomelic chondrodysplasia punctate type 4 |