Autosomal recessive polycystic kidney disease
Autosomal recessive polycystic kidney disease
Definition
An inherited disorder characterized by the development of cysts affecting the collecting ducts. It is frequently associated with hepatic involvement.
Also known as AR-PKD, ARPKD, autosomal recessive polycystic kidney, polycystic kidney disease, autosomal recessive, polycystic kidney disease, infantile type — per MONDO
Also identified as
- DOID 0110861 per MONDO
- ICD9 753.14 per MONDO
- NCIT C84579 per MONDO
- Orphanet 731 per MONDO
- SCTID 28770003 per MONDO
- UMLS C0085548 per MONDO
Affected Organs
| Organ | Involvement | Source |
|---|---|---|
| Adult mammalian kidney | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Adult mammalian kidney | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Genitourinary system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Genitourinary system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |
| Renal system | Disease Has Associated Anatomic Site | NCIT · CC BY 4.0 |
| Renal system | Disease Has Primary Anatomic Site | NCIT · CC BY 4.0 |