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MIM:616816 - HYPOTONIA, INFANTILE, WITH PSYCHOMOTOR RETARDATION; IHPMR
Xenbase Genes: ccdc174
Human Disease Resource: MIM
| MONDO:0014784 - severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome |
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| MONDO:0014784 - severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome |