Search Ontology:
Human Disease
hereditary spastic paraplegia 11
- Term ID
- DOID:0110764
- Synonyms
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- autosomal recessive spastic paraplegia 11
- autosomal recessive spastic paraplegia complicated with thin corpus callosum
- autosomal recessive spastic paraplegia type 11
- autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum
- HSP-TCC
- Nakamura-Osame syndrome
- spastic paraplegia-intellectual disability-thin corpus callosum syndrome
- SPG11
- Definition
- A hereditary spastic paraplegia that has_material_basis_in mutation in the SPG11 gene on chromosome 15q21. https://www.ncbi.nlm.nih.gov/pubmed/17322883
- References
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- GARD:4919
- ICD10CM:G11.4
- MIM:604360
- ORDO:2822
- Ontology
- Human Disease ( DOID:0110764 )
- is a type of
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