|
| General Information | |||
|---|---|---|---|
| Term | hereditary spastic paraplegia 18A | ID (Ontology) | DOID:0070640 (Human Disease) |
| Definition | A hereditary spastic paraplegia 18 that has_material_basis_in heterozygous mutation in the ERLIN2 gene on chromosome 8p11. | ||
| Also Known As | "autosomal dominant spastic paraplegia 18" ; "spastic paraplegia 18A" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
autosomal genetic disease |__autosomal dominant disease________ hereditary spastic paraplegia | |__hereditary spastic paraplegia 18__| hereditary spastic paraplegia 18A |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a |
autosomal dominant disease hereditary spastic paraplegia 18 |
||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
| MIM:620512 | |||