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46,XX Sex Reversal with Dysgenesis of Kidneys, Adrenals, and Lungs
AIDS-Associated Nephropathy
Alcoholic Liver Diseases +
alpha 1-antitrypsin deficiency
apolipoprotein A-IV associated amyloidosis
Arnold Stickler Bourne Syndrome
autoimmune interstitial lung, joint, and kidney disease
Bifid Nose with or without Anorectal and Renal Anomalies
BILIARY, RENAL, NEUROLOGIC, AND SKELETAL SYNDROME
BRAIN MALFORMATION RENAL SYNDROME
Carnitine Palmitoyltransferase II Deficiency, Infantile
cerebral amyloid angiopathy +
chronic congestive splenomegaly
Complement Factor H Deficiency
Cyanosis and Hepatic Disease
dialysis-related amyloidosis
Epidermolysis Bullosa Simplex 7, with Nephropathy and Deafness
familial juvenile hyperuricemic nephropathy +
Focal Nodular Hyperplasia
Glycogen Storage Disease 0, Liver
glycogen storage disease IX +
glycogen storage disease VI
granulomatosis with polyangiitis +
GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY
GSD IV, Nonprogressive Hepatic
Hantavirus hemorrhagic fever with renal syndrome +
hepatic vascular disease +
hepatosplenic schistosomiasis
Hydranencephaly with Renal Aplasia-Dysplasia
hypophosphatemic nephrolithiasis/osteoporosis +
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment
immunoglobulin heavy chain amyloidosis
immunoglobulin heavy-and-light chain
immunoglobulin light chain amyloidosis
Infundibulopelvic Dysgenesis
INTERSTITIAL LUNG AND LIVER DISEASE
intrahepatic cholestasis +
Jejunal Atresia with Renal Adysplasia
kidney papillary necrosis
Lachiewicz Sibley Syndrome
Lipoprotein Glomerulopathy
Liver Fibrocystic Disease and Polydactyly
liver inflammatory pseudotumor
Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus
mineral metabolism disease +
mitochondrial DNA depletion syndrome 6
nephrogenic diabetes insipidus +
neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES
Parasitic Liver Diseases +
Phosphoenolpyruvate Carboxykinase Deficiency +
polycystic echinococcosis
polycystic liver disease +
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease
Recurrent Infections, with Encephalopathy, Hepatic Dysfunction, and Cardiovascular Malformations
renal artery obstruction +
Renal Dysplasia - Limb Defects Syndrome
Renal Nutcracker Syndrome
Renal Tubular Dysgenesis +
renal tubular transport disease +
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia due to Duplication of Mitochondrial DNA
renal-hepatic-pancreatic dysplasia +
Retinohepatoendocrinologic Syndrome
secondary hyperparathyroidism of renal origin
Selig Benacerraf Greene Syndrome
serum amyloid A amyloidosis An amyloidosis that is characterized by sustained high levels of inflammatory serum amyloid A protein when inflammation is present in the body. (DO)
Severe Congenital Liver Disease
Siegler Brewer Carey Syndrome
Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy
steatotic liver disease +
stricture or kinking of ureter
Thrombocytopenia with Elevated Serum Iga and Renal Disease
Thyrocerebral-Retinal Syndrome
Trichohepatoneurodevelopmental Syndrome
variant ABeta2M amyloidosis
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