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Ontology Browser
Term:
Autosomal dominant medullary cystic kidney disease with hyperuricemia
(EFO:Orphanet:88950)
Annotations:
Rat: (0)
Mouse: (0)
Human: (0)
Chinchilla: (0)
Bonobo: (0)
Dog: (0)
Squirrel: (0)
Pig: (0)
Naked Mole-rat: (0)
Green Monkey: (0)
Parent Terms
Term With Siblings
Child Terms
kidney disease
+
Rare genetic renal disease
+
17q11 microdeletion syndrome
Acute hepatic porphyria
+
adenovirus renal infection
Adult familial nephronophthisis - spastic quadriparesia
Alpha-1-antitrypsin deficiency
anuria
atheroembolism of kidney
Autosomal dominant medullary cystic kidney disease with hyperuricemia
Autosomal dominant polycystic kidney disease
+
autosomal dominant progressive nephropathy with hypertension
Autosomal recessive infantile hypercalcemia
Behcet's syndrome
Brachydactyly - arterial hypertension
Cerebro-reno-digital syndrome
chronic kidney disease
+
Congenital disorder of glycosylation with nephropathy as a major feature
Congenital erythropoietic porphyria
congenital primary megaureter
+
cystic kidney disease
+
diabetes insipidus
+
duplication of urethra
exstrophy-epispadias complex
+
Familial porphyria cutanea tarda
+
fetal lower urinary tract obstruction
+
Genetic glomerular disease
+
Genetic renal or urinary tract malformation
+
Genetic renal tubular disease
+
Genetic thrombotic microangiopathy
glomerular disease
+
Glycogen storage disease due to glucose-6-phosphatase deficiency
+
Gräsbeck-Imerslund disease
hantavirus hemorrhagic fever with renal syndrome
+
Hematological disorder with renal involvement
+
hemoglobinuria
+
hemorrhagic fever with renal syndrome
Hepatic fibrosis - renal cysts - intellectual disability
hydronephrosis
+
hypertensive nephropathy
+
impaired renal function disease
+
Infantile nephronophthisis
inherited kidney disorder
+
Juvenile cataract - microcornea - renal glucosuria
Juvenile nephronophthisis
Juvenile nephropathic cystinosis
kidney cortex necrosis
kidney failure
+
kidney neoplasm
+
kidney papillary necrosis
+
nephritis
+
nephrocalcinosis
+
nephrolithiasis
+
nephrosis
+
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion
perinephritis
polymyositis
+
post-operative acute kidney injury
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia
Pseudoxanthoma elasticum
renal aminoaciduria
renal artery disease
+
renal dysplasia
+
Renal glucosuria
renal glycosuria
renal hypertension
+
renal hypoplasia
+
renal nutcracker syndrome
renal tuberculosis
+
renal tubular dysgenesis
+
renal tubular transport disease
+
renal tubule disease
+
sialidosis type II
+
stricture or kinking of ureter
systemic lupus erythematosus
+
systemic scleroderma
+
Takayasu arteritis
temporal arteritis
Tyrosinemia type 1
ureteral disorder
+
Vitamin B12-responsive methylmalonic acidemia type cblA
Vitamin B12-responsive methylmalonic acidemia type cblB
X-linked diffuse leiomyomatosis-Alport syndrome
X-linked erythropoietic protoporphyria
Zellweger syndrome
Synonyms
Xrefs:
ICD10:Q61.5
External Ontologys:
has_disease_location EFO:UBERON:0002113