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 +
poor metabolism of thiopurines +
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
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)

is-a denotes an 'is-a' relationship