WormBase Tree Display for DO_term: DOID:0110861
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| DOID:0110861 | Name | autosomal recessive polycystic kidney disease | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A polycystic kidney disease characterized by the presence of multiple cysts located_in the kidney resulting from ciliopathy that disrupts the function of primary cilium, inherited in an autosomal recessive fashion. | ||||
| Synonym | Exact | Arpkd | |||
| Pkhd1 | |||||
| Polycystic Kidney Disease, Infantile, Type I | |||||
| Polycystic Kidney and Hepatic Disease 1 | |||||
| Parent | Is_a | DOID:0050737 | |||
| DOID:0080322 | |||||
| Child | Is | DOID:0080212 | |||
| DOID:0080273 | |||||
| DB_info | Database | OMIM | disease | 263200 | |
| Attribute_of | Gene_by_orthology | WBGene00000387 | |||
| WBGene00000388 |
