Preferred Name |
Polycystic_Kidney_Disease_Infantile_Type |
|
Synonyms |
|
|
ID |
http://www.owl-ontologies.com/Ontology1358660052.owl#Polycystic_Kidney_Disease_Infantile_Type |
|
ID |
C84579 |
|
NCI_Definition |
Polycystic kidney disease inherited in an autosomal recessive pattern. Patients present with progressive renal failure early in life. The autosomal recessive trait is associated with abnormalities of chromosome 6. |
|
NCI_PT |
Autosomal Recessive Polycystic Kidney Disease |
|
NICHD_Definition |
_ |
|
prefixIRI |
Polycystic_Kidney_Disease_Infantile_Type |
|
prefLabel |
Polycystic_Kidney_Disease_Infantile_Type |
|
Subset_Association1 |
NICHD Pediatric Terminology |
|
Subset_Association2 |
Neonatal Research Network Terminology |
|
SYN | ||
subClassOf |
http://www.owl-ontologies.com/Ontology1358660052.owl#Autosomal_Recessive_Hereditary_Disorder |
Create mapping
Delete | Mapping To | Ontology | Source |
---|---|---|---|
http://purl.bioontology.org/ontology/SNOMEDCT/28770003 | SNOMEDCT | LOOM | |
http://purl.bioontology.org/ontology/SNMI/D4-71320 | SNMI | LOOM |