Parent term(s)
heart disease
+
liver disease
+
kidney disease
+
inherited metabolic disorder
+
amyloidosis
+
Term with siblings
immunoglobulin light chain amyloidosis
aceruloplasminemia
Alagille syndrome
alveolar echinococcosis
amino acid metabolic disorder
+
ankyrin-B-related cardiac arrhythmia
anuria
apolipoprotein A-IV associated amyloidosis
apolipoprotein A-IV associated amyloidosis
aromatic L-amino acid decarboxylase deficiency
atheroembolism of kidney
autoimmune cardiomyopathy
bilirubin metabolic disorder
+
capillariasis
carbohydrate metabolic disorder
+
cardiac tuberculosis
cardiomyopathy
+
cerebral amyloid angiopathy
+
cerebral amyloid angiopathy
+
clonorchiasis
congenital heart disease
+
congestive heart failure
+
cystic echinococcosis
cystic echinococcosis
cystic kidney disease
+
cysticercosis
cystinuria
D-glyceric aciduria
diabetes insipidus
+
dialysis-related amyloidosis
dialysis-related amyloidosis
dioctophymiasis
dopamine beta-hydroxylase deficiency
endocardium disease
+
familial hypocalciuric hypercalcemia
+
familial juvenile hyperuricemic nephropathy
familial visceral amyloidosis
familial visceral amyloidosis
glycerol kinase deficiency
Goodpasture syndrome
+
Gordon Holmes syndrome
granulomatosis with polyangiitis
Greenberg dysplasia
Hantavirus hemorrhagic fever with renal syndrome
+
heart aneurysm
+
heart cancer
+
heart conduction disease
+
heart lipoma
+
heart valve disease
+
hemolytic-uremic syndrome
hepatic tuberculosis
hepatic vascular disease
+
hepatitis
+
hepatopulmonary syndrome
heterophyiasis
HRPT-related hyperuricemia
hyperphosphatemic familial tumoral calcinosis
hypertensive heart disease
hypophosphatemic nephrolithiasis/osteoporosis
+
immunoglobulin heavy chain amyloidosis
immunoglobulin heavy chain amyloidosis
immunoglobulin heavy-and-light chain
infantile liver failure syndrome
+
isolated elevated serum creatine phosphokinase levels
isolated sulfite oxidase deficiency
kidney benign neoplasm
+
kidney cancer
+
kidney carcinoma in situ
kidney cortex disease
+
kidney failure
+
kidney hypertrophy
kidney papillary necrosis
lipid metabolism disorder
+
liver benign neoplasm
+
liver cancer
+
liver carcinoma in situ
liver cirrhosis
+
liver inflammatory pseudotumor
lysosomal storage disease
+
metal metabolism disorder
+
mitochondrial metabolism disease
+
multiple acyl-CoA dehydrogenase deficiency
nephritis
+
nephrocalcinosis
nephrolithiasis
+
nephronophthisis
+
obstructive nephropathy
opisthorchiasis
orthostatic proteinuria
paragonimiasis
perinephritis
peroxisomal disease
+
phosphoribosylpyrophosphate synthetase superactivity
plasma protein metabolism disease
+
polycystic echinococcosis
polycystic liver disease
+
porphyria
+
primary cutaneous amyloidosis
+
primary cutaneous amyloidosis
+
proteinuria
+
purine-pyrimidine metabolic disorder
+
pyelitis
+
pyrimidine metabolic disorder
+
renal agenesis
+
renal fibrosis
renal hypertension
+
renal hypoplasia
+
renal infectious disease
renal osteodystrophy
renal tuberculosis
renal tubular transport disease
+
secondary hyperparathyroidism of renal origin
serum amyloid A amyloidosis
serum amyloid A amyloidosis
serum amyloid A amyloidosis
steatotic liver disease
+
stricture or kinking of ureter
thiopurine S-methyltransferase deficiency
toxocariasis
toxocariasis
transient infantile liver failure
transthyretin amyloidosis
transthyretin amyloidosis
transthyretin amyloidosis
trimethylaminuria
tyrosinemia type II
variant ABeta2M amyloidosis
variant ABeta2M amyloidosis
visceral leishmaniasis
vitamin metabolic disorder
+
warfarin resistance
warfarin sensitivity
wild-type amyloidosis
wild-type amyloidosis
X-linked warfarin sensitivity
Child term(s)
denotes an 'is-a' relationship