loading...| Preferred Name |
Polycystic Kidney, Autosomal Recessive [Disease/Finding] |
|
| Synonyms |
Polycystic Kidney Disease, Autosomal Recessive |
|
| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000003520 |
|
| altLabel |
Polycystic Kidney Disease, Autosomal Recessive ARPKD Kidney, Polycystic, Autosomal Recessive Autosomal Recessive Polycystic Kidney Disease Polycystic Kidney Disease, Infantile, Type I Polycystic Kidney and Hepatic Disease 1 (Autosomal Recessive) Autosomal Recessive Polycystic Kidney Polycystic Kidney, Autosomal Recessive Polycystic Kidney Disease, Infantile, Type 1 Polycystic Kidney and Hepatic Disease 1 |
|
| cui |
C0085548 |
|
| MESH DEFINITION |
A genetic disorder with autosomal recessive inheritance, characterized by multiple CYSTS in both KIDNEYS and associated LIVER lesions. Serious manifestations are usually present at BIRTH with high PERINATAL MORTALITY. |
|
| MESH DUI |
D017044 |
|
| MeSH name |
Polycystic Kidney, Autosomal Recessive |
|
| MESH UI |
M0025899 |
|
| NDFRT kind |
DISEASE_KIND |
|
| notation |
N0000003520 |
|
| NUI |
N0000003520 |
|
| prefLabel |
Polycystic Kidney, Autosomal Recessive [Disease/Finding] |
|
| SNOMED CID |
28770003 |
|
| tui |
T047 |
|
| subClassOf |