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MIM:615491 - SPASTIC PARAPLEGIA 79B, AUTOSOMAL RECESSIVE; SPG79B
Xenbase Genes: uchl1
Human Disease Resource: MIM
MONDO:0014209 - early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome |
DOID:0112344 - hereditary spastic paraplegia 79B |