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Disease Ontology Browser
hereditary spastic paraplegia 86 (DOID:0112342)
Alliance: disease page
Synonyms: 'spastic paraplegia 86 autosomal recessive'; 'SPG86'
Alt IDs: OMIM:619735
Definition: A hereditary spastic paraplegia characterized by early childhood onset of global developmental delay and early-onset progressive spasticity mainly affecting the lower limbs but also affecting the upper lmbs that has_material_basis_in homozygous or compound heterozygous mutation in ABHD16A on chromosome 6p21.33.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
06/23/2022
MGI 6.20
The Jackson Laboratory