WormBase Tree Display for DO_term: DOID:905
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| DOID:905 | Name | Zellweger syndrome | |
|---|---|---|---|
| Status | Valid | ||
| Definition | A peroxisomal biogenesis disorder that is characterized by the reduction or absence of functional peroxisomes in the cells of an individual that has_material_basis_in autosomal recessive inheritance of a mutation in the peroxisome biogenesis factor (PEX) genes. | ||
| Comment | OMIM mapping confirmed by DO. | ||
| Synonym | Exact | cerebrohepatorenal syndrome | |
| congenital iron overload | |||
| Parent | Is_a | DOID:0050737 | |
| DOID:0080377 | |||
| Attribute_of | Gene_by_orthology | WBGene00003623 | |
| WBGene00004058 | |||
| WBGene00004059 | |||
| WBGene00013284 | |||
| WBGene00013999 | |||
| WBGene00014000 |
