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Disease association ontology term - MONDO:0012787 - hereditary spastic paraplegia 39

Term summary

ID
MONDO:0012787
Name
hereditary spastic paraplegia 39
Ontology or CV name
Disease association
Definition
This syndrome is characterized by progressive spastic paraplegia and distal muscle wasting.

Parents

Annotation

Disease association

MONDO:0012787 - hereditary spastic paraplegia 39

References:

Genes: