Search Ontology:
Human Disease

hereditary spastic paraplegia 18B

Term ID
DOID:0070641
Synonyms
  • spastic paraplegia 18B
Definition
A hereditary spastic paraplegia 18 that has_material_basis_in homozygous mutation in the ERLIN2 gene on chromosome 8p11. (2)
References
Ontology
Human Disease   ( DOID:0070641 )
Relationships
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Genes Involved
Zebrafish Models