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)

is-a denotes an 'is-a' relationship