ZFIN Human Disease: hereditary spastic paraplegia 28

OBO ID: DOID:0110779

Term Name:	hereditary spastic paraplegia 28		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 28 autosomal recessive spastic paraplegia type 28 SPG28
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
References:	ICD10CM:G11.4 OMIM:609340 ORDO:101008
Ontology:	Human Disease ( DOID:0110779 )

Relationships

is a type of:	autosomal recessive disease hereditary spastic paraplegia autosomal recessive disease hereditary spastic paraplegia Show first 5 Terms

OTHER hereditary spastic paraplegia 28 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
DDHD1	ddhd1b ddhd1a	Spastic paraplegia 28, autosomal recessive	609340

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None