ZFIN Human Disease: hereditary spastic paraplegia 2

OBO ID: DOID:0110773

Term Name:	hereditary spastic paraplegia 2		Search Ontology:
Synonyms:	spastic paraplegia type 2 SPG2 X-linked spastic paraplegia 2
Definition:	A hereditary spastic paraplegia that has_material_basis_in mutation in the PLP1 gene on chromosome Xq22.2. https://www.ncbi.nlm.nih.gov/pubmed/8012387
References:	GARD:4923 ICD10CM:G11.4 OMIM:312920 ORDO:99015
Ontology:	Human Disease ( DOID:0110773 )

Relationships

is a type of:	hereditary spastic paraplegia X-linked recessive disease hereditary spastic paraplegia X-linked recessive disease Show first 5 Terms

OTHER hereditary spastic paraplegia 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
PLP1	plp1b plp1a	Spastic paraplegia 2, X-linked	312920

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None