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hereditary spastic paraplegia 89
Summary
- Synonym
-
- SPG89
- autosomal recessive spastic paraplegia 89
- 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.
- Super Class
- autosomal recessive disease hereditary spastic paraplegia
External Links
- Disease Ontology
- DOID:0070458
- Mondo Disease Ontology
- OMIM
