WormBase Tree Display for DO_term: DOID:898
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DOID:898 | Name | autosomal dominant 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 dominant fashion. | ||
Comment | Xref MGI. | ||
Synonym | Exact | ADPKD | |
Congenital biliary ectasias | |||
POLYCYSTIC KIDNEY AND HEPATIC DISEASE 1 | |||
Parent | Is_a | DOID:0080322 | |
DOID:0050736 | |||
Child | Is | DOID:0110858 | |
DOID:0110859 | |||
DOID:0110860 | |||
Disease_model_annotation | WBDOannot00000024 | ||
WBDOannot00000030 | |||
WBDOannot00000033 | |||
WBDOannot00000512 | |||
WBDOannot00000513 | |||
WBDOannot00000514 | |||
WBDOannot00000515 | |||
WBDOannot00000516 | |||
WBDOannot00000517 | |||
Attribute_of | Gene_by_biology | WBGene00004035 | |
WBGene00003885 | |||
WBGene00003058 | |||
WBGene00002218 | |||
Gene_by_orthology (11) | |||
Disease_model_variation | WBVar00089148 | ||
WBVar00249009 | |||
WBVar00249016 | |||
WBVar00249018 | |||
WBVar00249002 |