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hereditary spastic paraplegia 9B

http://purl.obolibrary.org/obo/DOID_0110825

A hereditary spastic paraplegia that has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ALDH18A1 gene on chromosome 10q24. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

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Term info

Label

hereditary spastic paraplegia 9B

Synonyms

SPG9B
autosomal recessive complex spastic paraplegia type 9B
autosomal recessive spastic paraplegia 9B

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disease_ontology

DOID:0110825

Term relations

Subclass of:

autosomal recessive disease
hereditary spastic paraplegia
has material basis in some autosomal recessive inheritance