hereditary spastic paraplegia 89

Term ID

DOID:0070458

Synonyms

• autosomal recessive spastic paraplegia 89
• SPG89

Definition

A hereditary spastic paraplegia characterized by infantile or early childhood onset of lower limb spasticity that has_material_basis_in homozygous mutation in the AMFR gene on chromosome 16q13. https://pubmed.ncbi.nlm.nih.gov/37119330/

References

• OMIM:620379

Ontology

Human Disease   ( DOID:0070458 )