|
General Information
|
| Term |
hereditary spastic paraplegia 35 |
ID (Ontology) |
DOID:0110786 (Human Disease) |
| Definition |
A hereditary spastic paraplegia that has_material_basis_in mutation in the FA2H gene on chromosome 16q23.1. |
| Also Known As |
"autosomal recessive spastic paraplegia 35" ; "autosomal recessive spastic paraplegia type 35" ; "FAHN" (for all, see Synonyms field below) |
| Comment |
|
|
Links to External Ontologies
|
|
DO.org
|
|
Annotations
|
|
Records annotated with this term OR any of its CHILD TERMS
|
|
|
|
Records annotated with this exact term (annotations to child terms are NOT included)
|
| Data Class | Field | Records |
|---|
|
| Alleles (FBal) | HUMAN_DISEASE_INTERACTIONS | 3 | | Human Disease Models (FBhh) | DOID | 1 |
|
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
| Full annotation statements | Relevant FlyBase reports |
|---|
| Alleles | Genes | Human Disease Models |
|---|
hereditary spastic paraplegia 35 | 3 | 2 | 1 | ameliorates | hereditary spastic paraplegia 35 | 1 | -- | -- | for disease ribbon | hereditary spastic paraplegia 35 | -- | 1 | -- | model of | hereditary spastic paraplegia 35 | 2 | 1 | -- |
|
Relationships