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3-Hydroxyacyl-CoA Dehydrogenase Deficiency
46,XX Sex Reversal with Dysgenesis of Kidneys, Adrenals, and Lungs
6-Phosphogluconolactonase Deficiency
Acetylcarnitine Deficiency
Acid Phosphatase Deficiency
Acute Reversible Leukoencephalopathy with Increased Urinary Alpha-ketoglutarate
AIDS-Associated Nephropathy
Alpha-Fetoprotein Deficiency
Alpha-Fetoprotein, Hereditary Persistence of
amino acid metabolic disorder +
Amino Acid Transport Disorders, Inborn +
Angiotensin I-Converting Enzyme, Benign Serum Increase
apolipoprotein A-IV associated amyloidosis
Arene Oxide Detoxification Defect
Arnold Stickler Bourne Syndrome
aromatase excess syndrome
Aryl Hydrocarbon Hydroxylase Inducibility
autoimmune interstitial lung, joint, and kidney disease
Bifid Nose with or without Anorectal and Renal Anomalies
BILIARY, RENAL, NEUROLOGIC, AND SKELETAL SYNDROME
bilirubin metabolic disorder +
BRAIN MALFORMATION RENAL SYNDROME
Butyrylcholinesterase Deficiency
Butyrylcholinesterase Deficiency, Fluoride-Resistant, Japanese Type
carbohydrate metabolic disorder +
CARBONIC ANHYDRASE VA DEFICIENCY, HYPERAMMONEMIA DUE TO
Carnitine Acetyltransferase Deficiency
cerebral amyloid angiopathy +
CHITOTRIOSIDASE DEFICIENCY
Combined Congenital Deficiency of Intrinsic Factor and R Binder
Combined Defect of Growth Factors
Combined Exocrine Pancreatic Insufficiency
Combined Immunodeficiency and Megaloblastic Anemia with or without Hyperhomocysteinemia
Complement Factor H Deficiency
congenital leptin deficiency
congenital nonspherocytic hemolytic anemia 4
congenital nonspherocytic hemolytic anemia 5
congenital secretory chloride diarrhea 1
congenital secretory sodium diarrhea 3
Copper Deficiency, Familial Benign
Deafness Hyperuricemia Neurologic Ataxia
Decreased Urinary Activity of Kallikrein
Defect in Hyaluronan Metabolism
Defect in Hydroxylation of Diphenylhydantoin
Deficient N-Hydroxylation of Amobarbital
Deoxyribose-5-Phosphate Aldolase Deficiency
dialysis-related amyloidosis
dopamine beta-hydroxylase deficiency
DYSOSTOSIS MULTIPLEX, AIN-NAZ TYPE
Efavirenz, Poor Metabolism of
Epidermolysis Bullosa Simplex 7, with Nephropathy and Deafness
familial erythrocytosis 8
familial hypocalciuric hypercalcemia +
familial juvenile hyperuricemic nephropathy +
FUCOSYLTRANSFERASE 6 DEFICIENCY
Glucocorticoid Receptor Deficiency
Glucose-Stimulated Secretory Diarrhea, with Common Variable Immunodeficiency
Glycoprotein Storage Disease
granulomatosis with polyangiitis +
Hantavirus hemorrhagic fever with renal syndrome +
Hereditary Hyperbilirubinemia +
Hydranencephaly with Renal Aplasia-Dysplasia
Hypercalcemia, Infantile, 1
hyperphosphatemic familial tumoral calcinosis +
hypophosphatemic nephrolithiasis/osteoporosis +
Ichthyosis, Mental Retardation, Dwarfism, and Renal Impairment
immunoglobulin heavy chain amyloidosis
immunoglobulin light chain amyloidosis
Infundibulopelvic Dysgenesis
Inosine Triphosphatase Deficiency
isolated elevated serum creatine phosphokinase levels
isolated hyperchlorhidrosis
Jejunal Atresia with Renal Adysplasia
kidney papillary necrosis
Lachiewicz Sibley Syndrome
Lactate Dehydrogenase B Deficiency
Lactic Aciduria due to D-Lactic Acid
Leptin Receptor Deficiency
Leukotriene C4 Synthase Deficiency
lipid metabolism disorder +
Lipoprotein Glomerulopathy
Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus
lysosomal storage disease +
Mannose 6-Phosphate Receptor Recognition Defect, Lebanese Type
Mannose-Binding Protein Deficiency
Medium Chain 3-Ketoacyl-CoA Thiolase Deficiency
Metabolic Brain Diseases, Inborn +
metal metabolism disorder +
Methemoglobin Reductase Deficiency
Methylmalonyl-Coenzyme A Mutase Deficiency
mitochondrial metabolism disease +
Monocarboxylate Transporter 1 Deficiency
Monocyte Esterase Deficiency
Myeloperoxidase Deficiency
N Acetyltransferase Deficiency +
nephrogenic diabetes insipidus +
neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities
NEURODEVELOPMENTAL-CRANIOFACIAL SYNDROME WITH VARIABLE RENAL AND CARDIAC ABNORMALITIES
Nonfunctional L-Gulonolactone Oxidase
overhydrated hereditary stomatocytosis
Phenacetin O-Deethylase, Deficiency of
Phenol Sulfotransferase Deficiency
plasma protein metabolism disease +
Poor Drug Metabolism, CYP2C19-Related
Poor Drug Metabolism, CYP2D6-Related
Poor Metabolism of Proguanil
poor metabolism of thiopurines +
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease
purine-pyrimidine metabolic disorder +
pyrimidine metabolic disorder +
renal artery obstruction +
Renal Dysplasia - Limb Defects Syndrome
Renal Nutcracker Syndrome
Renal Tubular Dysgenesis +
renal tubular transport disease + Genetic defects in the selective or non-selective transport functions of the KIDNEY TUBULES.
Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia due to Duplication of Mitochondrial DNA
Retinol-Binding Protein Deficiency
secondary hyperparathyroidism of renal origin
SEDOHEPTULOKINASE DEFICIENCY
Selig Benacerraf Greene Syndrome
sepiapterin reductase deficiency
serum amyloid A amyloidosis
Siegler Brewer Carey Syndrome
Spastic Paraplegia, Sensorineural Deafness, Mental Retardation, and Progressive Nephropathy
Squalene Synthase Deficiency
stricture or kinking of ureter
SULFIDE:QUINONE OXIDOREDUCTASE DEFICIENCY
Thiamine Metabolism Dysfunction Syndrome 4 (Bilateral Striatal Degeneration and Progressive Polyneuropathy Type)
Thiamine Metabolism Dysfunction Syndrome 5 (Episodic Encephalopathy Type)
Thrombocytopenia with Elevated Serum Iga and Renal Disease
Thyrocerebral-Retinal Syndrome
Thyrotropin-Releasing Hormone Deficiency
Transcobalamin I Deficiency
type 1 diabetes mellitus 2
variant ABeta2M amyloidosis
vitamin metabolic disorder +
Weinstein Kliman Scully Syndrome
Wiedemann Oldigs Oppermann Syndrome
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