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Metadata
ID DOID:0110779
Name hereditary spastic paraplegia 28
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the DDHD1 gene on chromosome 14q22.
https://www.ncbi.nlm.nih.gov/pubmed/23176821
Xrefs

ICD10CM:G11.4

OMIM:609340

ORDO:101008

Subsets

DO_rare_slim

Synonyms

autosomal recessive spastic paraplegia 28 [EXACT]

autosomal recessive spastic paraplegia type 28 [EXACT]

SPG28 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

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