WormBase Tree Display for DO_term: DOID:0070347
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| DOID:0070347 | Name | encephalopathy due to defective mitochondrial and peroxisomal fission 1 | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A syndrome that has_material_basis_in heterozygous mutation in the DNM1L gene, and is characterized by delayed psychomotor development and has_symptom hypotonia that may lead to death in childhood. | ||||
| Parent | Is_a | DOID:225 | |||
| DB_info | Database | OMIM | disease | 614388 | |
| Attribute_of | Gene_by_orthology | WBGene00001093 |
