WormBase Tree Display for DO_term: DOID:0110808
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DOID:0110808 | Name | hereditary spastic paraplegia 56 | |||
---|---|---|---|---|---|
Status | Valid | ||||
Definition | A hereditary spastic paraplegia that has_material_basis_in mutation in the CYP2U1 gene on chromosome 4q25. | ||||
Synonym | Exact | SPG56 | |||
autosomal recessive spastic paraplegia 56 | |||||
autosomal recessive spastic paraplegia type 56 | |||||
Parent | Is_a | DOID:2476 | |||
DOID:0050737 | |||||
DB_info | Database | OMIM | disease | 615030 | |
Attribute_of | Gene_by_orthology | WBGene00000373 | |||
WBGene00010589 | |||||
WBGene00010705 | |||||
WBGene00010706 | |||||
WBGene00010707 | |||||
WBGene00011009 | |||||
WBGene00012448 | |||||
WBGene00015709 | |||||
WBGene00016092 |