ZFIN Human Disease: hereditary spastic paraplegia 9B

OBO ID: DOID:0110825

Term Name:	hereditary spastic paraplegia 9B		Search Ontology:
Synonyms:	autosomal recessive complex spastic paraplegia type 9B autosomal recessive spastic paraplegia 9B SPG9B
Definition:	A hereditary spastic paraplegia that has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ALDH18A1 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/26026163
References:	ICD10CM:G11.4 OMIM:616586 ORDO:447760
Ontology:	Human Disease ( DOID:0110825 )

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 9B PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ALDH18A1	aldh18a1	Spastic paraplegia 9B, autosomal recessive	616586

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None