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MIM:615877 - MICROPHTHALMIA/COLOBOMA AND SKELETAL DYSPLASIA SYNDROME; MCSKS
Xenbase Genes: mab21l2
Human Disease Resource: MIM
| MONDO:0014380 - colobomatous microphthalmia-rhizomelic dysplasia syndrome |
| DOID:0111802 - syndromic microphthalmia 14 |
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| MONDO:0014380 - colobomatous microphthalmia-rhizomelic dysplasia syndrome |
| DOID:0111802 - syndromic microphthalmia 14 |