ZFIN Human Disease: hereditary spastic paraplegia 41

OBO ID: DOID:0110793

OBO ID: DOID:0110793

Term Name:	hereditary spastic paraplegia 41	Search Ontology:
Synonyms:	autosomal dominant spastic paraplegia 41 autosomal dominant spastic paraplegia type 41 SPG41
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 11p14.1-p11.2. https://www.ncbi.nlm.nih.gov/pubmed/18364116
References:	ICD10CM:G11.4 OMIM:613364 ORDO:320355
Ontology:	Human Disease ( DOID:0110793 )

Relationships

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

OTHER hereditary spastic paraplegia 41 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None