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46,XX Sex Reversal with Dysgenesis of Kidneys, Adrenals, and Lungs
AIDS-Associated Nephropathy
alcohol-associated liver disease +
alpha 1-antitrypsin deficiency
apolipoprotein A-IV associated amyloidosis
Arnold Stickler Bourne Syndrome
autoimmune interstitial lung, joint, and kidney disease
autosomal dominant tubulointerstitial 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
Craniofaciocardiohepatic syndrome
Cyanosis and Hepatic Disease
dialysis-related amyloidosis
Epidermolysis Bullosa Simplex 7, with Nephropathy and Deafness
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 +
polyomavirus-associated nephropathy
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease
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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