ZFIN Human Disease: hereditary spastic paraplegia 36

OBO ID: DOID:0110787

OBO ID: DOID:0110787

Term Name:	hereditary spastic paraplegia 36	Search Ontology:
Synonyms:	autosomal dominant spastic paraplegia 36 autosomal dominant spastic paraplegia type 36 SPG36
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 12q23-q24. https://www.ncbi.nlm.nih.gov/pubmed/19357379
References:	ICD10CM:G11.4 OMIM:613096 ORDO:320365
Ontology:	Human Disease ( DOID:0110787 )

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 36 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None