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Human Disease

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
Ontology
Human Disease   ( DOID:0070458 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models