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MIM:616901 - DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FACIAL FEATURES, AND SPARSE HAIR 1; DEDSSH1
Xenbase Genes: dph1
Human Disease Resource: MIM
DOID:0070477 - diphthamide deficiency syndrome 1 |
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DOID:0070477 - diphthamide deficiency syndrome 1 |