SPASTIC PARAPLEGIA 79B, AUTOSOMAL RECESSIVE; SPG79B

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Summary

Literature (0)

MIM:615491 - SPASTIC PARAPLEGIA 79B, AUTOSOMAL RECESSIVE; SPG79B

Xenbase Genes: uchl1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014209 - early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome

MONDO:0014209 - early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome

Disease Ontology (DO):

DOID:0112344 - hereditary spastic paraplegia 79B

DOID:0112344 - hereditary spastic paraplegia 79B