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Term:
Parent Terms Term With Siblings Child Terms
17q11 microdeletion syndrome 
Acute hepatic porphyria +  
Adult familial nephronophthisis - spastic quadriparesia 
Alpha-1-antitrypsin deficiency 
Autosomal dominant medullary cystic kidney disease with hyperuricemia 
Autosomal dominant polycystic kidney disease +  
Autosomal recessive infantile hypercalcemia 
Brachydactyly - arterial hypertension 
Congenital disorder of glycosylation with nephropathy as a major feature 
Congenital erythropoietic porphyria 
congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization 
Familial porphyria cutanea tarda +  
fibronectin glomerulopathy +  
Genetic glomerular disease +  
Genetic renal or urinary tract malformation +  
Genetic renal tubular disease +  
Genetic thrombotic microangiopathy 
glomerulonephritis +   
glomerulosclerosis +   
Glycogen storage disease due to glucose-6-phosphatase deficiency +  
Gräsbeck-Imerslund disease 
Hematological disorder with renal involvement +  
Hepatic fibrosis - renal cysts - intellectual disability 
Infantile nephronophthisis 
Juvenile cataract - microcornea - renal glucosuria 
Juvenile nephronophthisis 
Juvenile nephropathic cystinosis 
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion 
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia 
Pseudoxanthoma elasticum 
Renal glucosuria 
sialidosis type II +  
Tyrosinemia type 1 
Vitamin B12-responsive methylmalonic acidemia type cblA 
Vitamin B12-responsive methylmalonic acidemia type cblB 
X-linked erythropoietic protoporphyria 
Zellweger syndrome 

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