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| Term | autosomal recessive polycystic kidney disease | ID (Ontology) | DOID:0110861 (Human Disease) |
| 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. | ||
| Also Known As | "AR-PKD" | ||
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autosomal genetic disease |__autosomal recessive disease__ cystic kidney disease | |__polycystic kidney disease____| autosomal recessive polycystic kidney disease 1 rec. |__polycystic kidney disease 4 |__polycystic kidney disease 5 1 rec. |
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autosomal recessive disease polycystic kidney disease |
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GARD:8378 ICD10CM:Q61.1 ICD9CM:753.14 MESH:D017044 NCI:C84579 ORDO:731 SNOMEDCT_US_2023_03_01:28770003 UMLS_CUI:C0085548 |
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