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MIM:616756 - SPASTIC PARAPLEGIA AND PSYCHOMOTOR RETARDATION WITH OR WITHOUT SEIZURES; SPPRS
Xenbase Genes: hace1
Human Disease Resource: MIM
| MONDO:0014764 - spastic paraplegia-severe developmental delay-epilepsy syndrome |
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| MONDO:0014764 - spastic paraplegia-severe developmental delay-epilepsy syndrome |