ZFIN Human Disease: hereditary spastic paraplegia 34

OBO ID: DOID:0110785

OBO ID: DOID:0110785

Term Name:	hereditary spastic paraplegia 34	Search Ontology:
Synonyms:	SPG34 X-linked spastic paraplegia 34 X-linked spastic paraplegia type 34
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region Xq24-q25. https://www.ncbi.nlm.nih.gov/pubmed/12210342
References:	ICD10CM:G11.4 OMIM:300750 ORDO:171607
Ontology:	Human Disease ( DOID:0110785 )

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 34 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None