Disease association ontology term - MONDO:0014020 - hereditary spastic paraplegia 55

Term summary

ID: MONDO:0014020
Name: hereditary spastic paraplegia 55
Ontology or CV name: Disease association

Parents

is_a complex hereditary spastic paraplegia
is_a mitochondrial oxidative phosphorylation disorder

Annotation

Disease association

MONDO:0014020 - hereditary spastic paraplegia 55

References:

PB_REF:0000006

Genes:

pth3 (SPBC1105.18c)