Visualize Submit Comment
Metadata
ID DOID:0110802
Name hereditary spastic paraplegia 50
Definition A hereditary spastic paraplegia that has_material_basis_in mutation in the AP4M1 gene on chromosome 7q22.1.
https://www.ncbi.nlm.nih.gov/books/NBK535153/, https://www.ncbi.nlm.nih.gov/pubmed/19559397
Xrefs

OMIM:612936

ORDO:280763

Subsets

DO_rare_slim

Synonyms

adaptor protein complex 4 deficiency [EXACT]

AP-4 deficiency syndrome [EXACT]

AP-4-Associated Hereditary Spastic Paraplegia [EXACT]

autosomal recessive spastic paraplegia 50 [EXACT]

SPG50 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

Add an item to the term tracker