ZFIN Human Disease: hereditary spastic paraplegia 16

OBO ID: DOID:0110769

OBO ID: DOID:0110769

Term Name:	hereditary spastic paraplegia 16	Search Ontology:
Synonyms:	SPG16 X-linked spastic paraplegia 16 X-linked spastic paraplegia type 16
Definition:	A hereditary spastic paraplegia that has_material_basis_in variation in the chromosome region Xq11.2. https://www.ncbi.nlm.nih.gov/pubmed/9254866
References:	GARD:9585 ICD10CM:G11.4 OMIM:300266 ORDO:100997
Ontology:	Human Disease ( DOID:0110769 )

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 16 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None