ZFIN Human Disease: hereditary spastic paraplegia 49

OBO ID: DOID:0110801

Term Name:	hereditary spastic paraplegia 49		Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 49 autosomal recessive spastic paraplegia type 49 SPG49
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the TECPR2 gene on chromosome 14q32. https://www.ncbi.nlm.nih.gov/pubmed/23176824
References:	ICD10CM:G11.4 OMIM:615031 ORDO:320385
Ontology:	Human Disease ( DOID:0110801 )

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 49 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TECPR2	tecpr2	Neuropathy, hereditary sensory and autonomic, type IX, with developmental delay	615031

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None