WormBase Tree Display for DO_term: DOID:0110737
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| DOID:0110737 | Name | neurodegeneration with brain iron accumulation 3 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal dominant inheritance of mutation in the FTL gene on chromosome 19q13.33. | ||||
| Synonym | Exact | Adult basal ganglia disease | |||
| Ferritin-related neurodegeneration | |||||
| Hereditary ferritinopathy | |||||
| NBIA3 | |||||
| Neuroferritinopathy | |||||
| Neuroferritinopathy; Basal Ganglia Disease, Adult-Onset | |||||
| Parent | Is_a | DOID:0050736 | |||
| DOID:0110734 | |||||
| DB_info | Database | OMIM | disease | 606159 | |
| Attribute_of | Gene_by_orthology | WBGene00001500 | |||
| WBGene00001501 |
