ZFIN Human Disease: hereditary spastic paraplegia 23

OBO ID: DOID:0110774

Term Name:	hereditary spastic paraplegia 23		Search Ontology:
Synonyms:	Lison syndrome Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome spastic paraplegia 23 spastic paraplegia with pigmentary abnormalities SPG23
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 1q24-q32. https://www.ncbi.nlm.nih.gov/pubmed/14681889
References:	GARD:336 ICD10CM:G11.4 OMIM:270750 ORDO:101003
Ontology:	Human Disease ( DOID:0110774 )

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 23 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
DSTYK	dstyk	Spastic paraplegia 23, autosomal recessive	270750

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None