ZFIN Human Disease: hereditary spastic paraplegia 32

OBO ID: DOID:0110783

OBO ID: DOID:0110783

Term Name:	hereditary spastic paraplegia 32	Search Ontology:
Synonyms:	autosomal recessive spastic paraplegia 32 autosomal recessive spastic paraplegia type 32 SPG32
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region 14q12-q21. https://www.ncbi.nlm.nih.gov/pubmed/17515546
References:	GARD:12749 ICD10CM:G11.4 OMIM:611252 ORDO:171622
Ontology:	Human Disease ( DOID:0110783 )

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 32 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None