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MIM:616617 - HEIMLER SYNDROME 2; HMLR2
Xenbase Genes: pex6
Human Disease Resource: MIM
| MONDO:0014709 - obsolete Heimler syndrome 2 |
| MONDO:0100229 - obsolete Heimler syndrome |
| DOID:0080624 - Heimler syndrome 2 |
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| MONDO:0014709 - obsolete Heimler syndrome 2 |
| MONDO:0100229 - obsolete Heimler syndrome |
| DOID:0080624 - Heimler syndrome 2 |