ZFIN Human Disease: hereditary spastic paraplegia 27

OBO ID: DOID:0110778

OBO ID: DOID:0110778

Term Name:	hereditary spastic paraplegia 27	Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 27 autosomal recessive spastic paraplegia type 27 SPG27
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 10q22.1-q24.1. https://www.ncbi.nlm.nih.gov/pubmed/15455396
References:	ICD10CM:G11.4 OMIM:609041 ORDO:101007
Ontology:	Human Disease ( DOID:0110778 )

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 27 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None