shipment Shipment symptoms Inheritable symptom: Malformations of the urinary tract Inheritable symptom: Rickets Inheritable symptom: Osteoporosis Alphabetic index Inheritable symptom: Polyhydramnios Inheritable symptom: Hypokalemia Inheritable symptom: Hyperkalemia Inheritable symptom: Hypertension Inheritable symptom: Renal cysts Inheritable symptom: Hypophosphatemia Inheritable symptom: Deafness Inheritable symptom: Polyuria Inheritable symptom: Hypotension Inheritable symptom: Alkalosis Inheritable symptom: Glucosuria Inheritable symptom: Proteinuria Inheritable symptom: Hypercalcemia Inheritable symptom: Hypomagnesaemia Inheritable symptom: Osteopetrosis Inheritable symptom: Proximal tubular damage syndrome Inheritable symptom: Osteomalacia Inheritable symptom: Hypocalcemia Inheritable symptom: Acidosis Inheritable symptom: Kidney tumor Inheritable symptom: Urolithiasis and nephrocalcinosis Inheritable symptom: Growth retardation Inheritable symptom: Hematuria Inheritable symptom: Ocular abnormalities genes Molecular genetic analysis (gene test): Claudin 16 (CLDN16) Molecular genetic analysis (gene test): ARGININE VASOPRESSIN RECEPTOR 2 (AVPR2) Alphabetic index Molecular genetic analysis (gene test): Protein kinase, lysin-deficient 1 (WNK1) Molecular genetic analysis (gene test): Kidney chloride channel A (CLCNKA) Molecular genetic analysis (gene test): SLC34A3 solute carrier family 34 (sodium phosphate), member 3 (SLC34A3) Molecular genetic analysis (gene test): SODIUM BICARBONATE COTRANSPORTER 1 (SLC4A4) Molecular genetic analysis (gene test): Transactivator NEUROD1 (NEUROD1) Molecular genetic analysis (gene test): HADH gene (HADH) Molecular genetic analysis (gene test): Cytochrome P450, family 4, subfamily F, polypeptide 2 (CYP4F2) Molecular genetic analysis (gene test): Vacuolar protein pump, subunit 2 (ATP6V0A4) Molecular genetic analysis (gene test): Cytochrome P450, family 24, subfamily A, polypeptide 1 (CYP24A1) Molecular genetic analysis (gene test): Fumarate hydratase (FH) Molecular genetic analysis (gene test): Retinoid X receptor, alpha (RXRA) Molecular genetic analysis (gene test): Collagen, type IV, alpha 1 (COL4A1) Molecular genetic analysis (gene test): BBS7 gene (BBS7) Molecular genetic analysis (gene test): Complement factor H-related 1 (CFHR1) Molecular genetic analysis (gene test): AQUAPORIN 2 (AQP2) Molecular genetic analysis (gene test): Paired box 6 gene (PAX6) Molecular genetic analysis (gene test): BBS1 gene (BBS1) Molecular genetic analysis (gene test): Complement factor I (CFI) Molecular genetic analysis (gene test): Prothrombin (F2) Molecular genetic analysis (gene test): Oxidative stress-responsive 1 protein (OXSR1) Molecular genetic analysis (gene test): Methylenetetrahydrofolate reductase (MTHFR) Molecular genetic analysis (gene test): Complement component 1, q subcomponent, B chain (C1QB) Molecular genetic analysis (gene test): MSH2 gene (MSH2) Molecular genetic analysis (gene test): Hormone sensing transcription factor PPARG (PPARG) Molecular genetic analysis (gene test): Cystinuria gene 2 (SLC7A9) Molecular genetic analysis (gene test): Solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15 (SLC25A15) Molecular genetic analysis (gene test): Glyoxylate reductase/hydroxypyruvate reductase (GRHPR) Molecular genetic analysis (gene test): V-KI-RAS2 Kirsten rat sarcoma viral oncogene homolog (KRAS) Molecular genetic analysis (gene test): Sodium-glucose transporter 2 (SLC5A2) Molecular genetic analysis (gene test): Calcium sensing receptor (CASR) Molecular genetic analysis (gene test): Renal outer-medullary potassium channel (KCNJ1) Molecular genetic analysis (gene test): Epidermal growth factor (EGF) Molecular genetic analysis (gene test): VACUOLAR PROTON PUMP, SUBUNIT 3 (ATP6V1B1) Molecular genetic analysis (gene test): Arginine vasopressin (AVP) Molecular genetic analysis (gene test): POLYCYSTIN 1 (PKD1) Molecular genetic analysis (gene test): Potassium inwardly-rectifying channel, subfamily J, member 10 (KCNJ10) Molecular genetic analysis (gene test): CDGSH iron sulfur domain 2 (CISD2) Molecular genetic analysis (gene test): Hyaluronan-binding protein 2 (HABP2) Molecular genetic analysis (gene test): Alanine-glyoxylate aminotransferase (AGXT) Molecular genetic analysis (gene test): Insulin receptor (INSR) Molecular genetic analysis (gene test): Syntaxin 16 (STX16) Molecular genetic analysis (gene test): Nephrin (NPHS1) Molecular genetic analysis (gene test): Polycystin 2 (PKD2) Molecular genetic analysis (gene test): Laminin beta-2 (LAMB2) Molecular genetic analysis (gene test): Urate transporter (SLC22A12) Molecular genetic analysis (gene test): Chemokine, CC motif, receptor 5 (CCR5) Molecular genetic analysis (gene test): 25-hydroxyvitamin D3 1-alpha-hydroxylase gene (CYP27B1) Molecular genetic analysis (gene test): Complement factor H-related 2 (CFHR2) Molecular genetic analysis (gene test): Complement factor H-related 3 (CFHR3) Molecular genetic analysis (gene test): Apolipoprotein E (APOE) Molecular genetic analysis (gene test): Carboxyl ester lipase (CEL) Molecular genetic analysis (gene test): GROWTH HORMONE 1 (GH1) Molecular genetic analysis (gene test): Sodium-potassium-chloride transporter 2 (SLC12A1) Molecular genetic analysis (gene test): BBS4 gene (BBS4) Molecular genetic analysis (gene test): Hypoxanthine phosphoribosyltransferase 1 (HPRT1) Molecular genetic analysis (gene test): Sialin (SLC17A5) Molecular genetic analysis (gene test): Actinin alpha-4 (ACTN4) Molecular genetic analysis (gene test): Polycystic kidney and hepatic disease 1 gene (PKHD1) Molecular genetic analysis (gene test): BBS12 gene (BBS12) Molecular genetic analysis (gene test): Potassium channel, inwardly rectifying, subfamily J, member 11 (KCNJ11) Molecular genetic analysis (gene test): TRPC6 gene (TRPC6) Molecular genetic analysis (gene test): Collagen type IV, alpha 5 (COL4A5) Molecular genetic analysis (gene test): BBS8 gene (TTC8) Molecular genetic analysis (gene test): Apolipoprotein B (APOB) Molecular genetic analysis (gene test): Fibroblast growth factor 23 (FGF23) Molecular genetic analysis (gene test): Transcriptionfactor PAX4 (PAX4) Molecular genetic analysis (gene test): Amiloride binding protein 1 (amine oxidase (copper-containing)) (ABP1) Molecular genetic analysis (gene test): BBS2 gene (BBS2) Molecular genetic analysis (gene test): Platelet glycoprotein 1b alpha polypeptide (GP1BA) Molecular genetic analysis (gene test): Angiotensin II receptor, type 1 (AGTR1) Molecular genetic analysis (gene test): Argininosuccinate synthetase (ASS1) Molecular genetic analysis (gene test): Lipoprotein lipase (LPL) Molecular genetic analysis (gene test): WD repeat containing planar cell polarity effector (WDPCP) Molecular genetic analysis (gene test): Insulin promoter factor 1 (PDX1) Molecular genetic analysis (gene test): Myosin IE (MYO1E) Molecular genetic analysis (gene test): Transcription factor HNF1beta (HNF1B) Molecular genetic analysis (gene test): Lecithin-cholesterol acyltransferase (LCAT) Molecular genetic analysis (gene test): OCRL gene (OCRL1) Molecular genetic analysis (gene test): Cortisol 11-beta-ketoreductase (HSD11B2) Molecular genetic analysis (gene test): Cystinosis, nephropathic (CTNS) Molecular genetic analysis (gene test): Amino acid transporter responsible for LPI (SLC7A7) Molecular genetic analysis (gene test): Angiotensin converting enzyme 2 (ACE2) Molecular genetic analysis (gene test): Centrosomal protein, 290-KD (CEP290) Molecular genetic analysis (gene test): Epidermal growth factor receptor (EGFR) Molecular genetic analysis (gene test): Integrin, beta-3 (ITGB3) Molecular genetic analysis (gene test): CD2-associated protein (CD2AP) Molecular genetic analysis (gene test): SLC25A13 solute carrier family 25, member 13 (citrin) (SLC25A13) Molecular genetic analysis (gene test): Collagen type IV, alpha 3 (COL4A3) Molecular genetic analysis (gene test): UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase (GNE) Molecular genetic analysis (gene test): SIX homeobox 5 (SIX5) Molecular genetic analysis (gene test): BBS3 gene (ARL6) Molecular genetic analysis (gene test): Cytochrome P450, family 2, subfamily C, polypeptide 9 (CYP2C9) Molecular genetic analysis (gene test): Uromodulin (UMOD) Molecular genetic analysis (gene test): Von Willebrand factor-cleaving protease (ADAMTS13) Molecular genetic analysis (gene test): Platelet glycoprotein 1b beta polypeptide (GP1BB) Molecular genetic analysis (gene test): Protein S (PROS1) Molecular genetic analysis (gene test): Thrombomodulin (THBD) Molecular genetic analysis (gene test): Complement factor H (CFH) Molecular genetic analysis (gene test): Cytochrome P450, family 2, subfamily R, polypeptide 1 (CYP2R1) Molecular genetic analysis (gene test): Wolfram syndrome 1 gene (WFS1) Molecular genetic analysis (gene test): Transcriptionfactor KLF11 (KLF11) Molecular genetic analysis (gene test): Aldosterone synthase (CYP11B2) Molecular genetic analysis (gene test): MEMBRANE COFACTOR PROTEIN (MCP) Molecular genetic analysis (gene test): BBS10 gene (BBS10) Molecular genetic analysis (gene test): GNAS complex locus (GNAS) Molecular genetic analysis (gene test): Insulin (INS) Molecular genetic analysis (gene test): Methionine adenosyltransferase I alpha (MAT1A) Molecular genetic analysis (gene test): ALDOSE REDUCTASE (AKR1B1) Molecular genetic analysis (gene test): CCAAT/Enhancer-binding protein (CEBPA) Molecular genetic analysis (gene test): Nephrocystin 1 (NPHP1) Molecular genetic analysis (gene test): SODIUM CHANNEL, NONVOLTAGE-GATED 1, ALPHA SUBUNIT (SCNN1A) Molecular genetic analysis (gene test): Angiotensinogen (AGT) Molecular genetic analysis (gene test): Sulfonylurea receptor (ABCC8) Molecular genetic analysis (gene test): Inversin (INVS) Molecular genetic analysis (gene test): Sodium-glucose transporter 1 (SLC5A1) Molecular genetic analysis (gene test): Vascular endothelial growth factor (VEGFA) Molecular genetic analysis (gene test): Paraoxonase 1 (PON1) Molecular genetic analysis (gene test): ANTITHROMBIN 3 (SERPINC1) Molecular genetic analysis (gene test): BBS9 gene (PTHB1) Molecular genetic analysis (gene test): Histamine N-methyltransferase (HNMT) Molecular genetic analysis (gene test): Glutamate dehydrogenase 1 (GLUD1) Molecular genetic analysis (gene test): GATA binding protein 3 (GATA3) Molecular genetic analysis (gene test): Dentin matrix acidic phosphoprotein 1 (DMP1) Molecular genetic analysis (gene test): BBS6 gene (MKKS) Molecular genetic analysis (gene test): Renin (REN) Molecular genetic analysis (gene test): Eyes absent, drosophila homolog 1 (EYA1) Molecular genetic analysis (gene test): NEURAL PRECURSOR CELL EXPRESSED, DEVELOPMENTALLY DOWNREGULATED 4 (NEDD4) Molecular genetic analysis (gene test): Low density lipoprotein receptor (LDLR) Molecular genetic analysis (gene test): Integrin, alpha-2B (ITGA2B) Molecular genetic analysis (gene test): LIM homeobox transcription factor 1 beta (LMX1B) Molecular genetic analysis (gene test): SWI/SNF-related, matrix-associated, actin-dependent regulator of chromatin (SMARCAL1) Molecular genetic analysis (gene test): Hemochromatosis gene (HFE) Molecular genetic analysis (gene test): Thiazide-sensitive NA-CL Cotransporter (SLC12A3) Molecular genetic analysis (gene test): Nephrocystin 4 (NPHP4) Molecular genetic analysis (gene test): Podocin (NPHS2) Molecular genetic analysis (gene test): Transcription factor GCMB (GCM2) Molecular genetic analysis (gene test): BBS11 gene (TRIM32) Molecular genetic analysis (gene test): Serine threonine kinase 39 (STK39) Molecular genetic analysis (gene test): Gene of autosomal recessive hypercholesterolemia (LDLRAP1) Molecular genetic analysis (gene test): Complement component 3 (C3) Molecular genetic analysis (gene test): Glucose transporter 2 (SLC2A2) Molecular genetic analysis (gene test): Phosphatidylinositol glycan anchor biosynthesis, class A (PIGA) Molecular genetic analysis (gene test): Cytochrome P450, family 2, subfamily A, polypeptide 6 (CYP2A6) Molecular genetic analysis (gene test): MLH1 gene (MLH1) Molecular genetic analysis (gene test): Solute carrier family 26, member 6 (SLC26A6) Molecular genetic analysis (gene test): CARBONIC ANHYDRASE 2 (CA2) Molecular genetic analysis (gene test): Protein kinase, lysin-deficient 4 (WNK4) Molecular genetic analysis (gene test): Platelet glycoprotein IX (GP9) Molecular genetic analysis (gene test): MKS1 Gene (MKS1) Molecular genetic analysis (gene test): Transient receptor potential cation channel, subfamily M, member 7 (TRPM7) Molecular genetic analysis (gene test): Chloride channel 5 (CLCN5) Molecular genetic analysis (gene test): Zinc finger protein 57 (ZFP57) Molecular genetic analysis (gene test): Vitamin D receptor (VDR) Molecular genetic analysis (gene test): Growth hormone releasing hormone receptor (GHRHR) Molecular genetic analysis (gene test): Transcription factor HNF1alpha (HNF1A) Molecular genetic analysis (gene test): Channel kinase 2 (TRPM6) Molecular genetic analysis (gene test): Claudin 19 (CLDN19) Molecular genetic analysis (gene test): Epithelial sodium channel, gamma subunit (SCNN1G) Molecular genetic analysis (gene test): Apolipoprotein C2 (APOC2) Molecular genetic analysis (gene test): BBS5 gene (BBS5) Molecular genetic analysis (gene test): Collagen, type IV, alpha 2 (COL4A2) Molecular genetic analysis (gene test): Myocilin (MYOC) Molecular genetic analysis (gene test): Complement factor H-related 4 (CFHR4) Molecular genetic analysis (gene test): Protein C (PROC) Molecular genetic analysis (gene test): Angiotensin I-converting enzyme (ACE) Molecular genetic analysis (gene test): FXYD domain-containing ion transport regulator 2 (FXYD2) Molecular genetic analysis (gene test): Phospholipase C, epsilon-1 (PLCE1) Molecular genetic analysis (gene test): Wilms tumor 1 gene (WT1) Molecular genetic analysis (gene test): Gamma-glutamyl carboxylase (GGCX) Molecular genetic analysis (gene test): ANION EXCHANGE PROTEIN 1 (SLC4A1) Molecular genetic analysis (gene test): Nephrocystin 3 (NPHP3) Molecular genetic analysis (gene test): Cystinuria gene 1 (SLC3A1) Molecular genetic analysis (gene test): Complement factor H-related 5 (CFHR5) Molecular genetic analysis (gene test): ALMS1 gene (ALMS1) Molecular genetic analysis (gene test): Phospholipase A2 receptor 1 (PLA2R1) Molecular genetic analysis (gene test): Vitamin K epoxide reductase complex, subunit 1 (VKORC1) Molecular genetic analysis (gene test): Transcription factor HNF4alpha (HNF4A) Molecular genetic analysis (gene test): Kidney chloride channel B (CLCNKB) Molecular genetic analysis (gene test): Ubiquitin protein ligase NEDD4-like (NEDD4L) Molecular genetic analysis (gene test): Activin A receptor, type I (ACVR1) Molecular genetic analysis (gene test): Steroid 11-beta-hydroxylase (CYP11B1) Molecular genetic analysis (gene test): Inverted formin, FH2 and WH2 domain containing (INF2) Molecular genetic analysis (gene test): Complement factor B (CFB) Molecular genetic analysis (gene test): Alpha-galactosidase A (GLA) Molecular genetic analysis (gene test): Phosphate-regulating endopeptidase homolog, x-linked (PHEX) Molecular genetic analysis (gene test): Collagen type IV, alpha 4 (COL4A4) Molecular genetic analysis (gene test): Ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) Molecular genetic analysis (gene test): Glucokinase (GCK) Molecular genetic analysis (gene test): Barttin (BSND) Molecular genetic analysis (gene test): Mineralocorticoid receptor (NR3C2) Molecular genetic analysis (gene test): Coagulation factor 5 (F5) Molecular genetic analysis (gene test): Adenin phosphoribosyltransferase (APRT) Molecular genetic analysis (gene test): Cytochrome P450, subfamily IID, polypeptide 6 (CYP2D6) Molecular genetic analysis (gene test): Nonmuscle myosin heavy chain 9 (MYH9) Molecular genetic analysis (gene test): Epithelial sodium channel, beta subunit (SCNN1B) Molecular genetic analysis (gene test): Bruton agammaglobulinemia tyrosine kinase (BTK) Molecular genetic analysis (gene test): Cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) Molecular genetic analysis (gene test): Low density lipoprotein receptor-related protein 2 (LRP2) Molecular genetic analysis (gene test): Parathyroid hormone (PTH) diseases Hereditary disease: Bronchiectasis with or without elevated sweat chloride 1 Hereditary disease: Inclusion body myopathy 2 Hereditary disease: Kidney disease appearing as endocrinological disorders Hereditary disease: Pierson syndrome Alphabetic index Hereditary disease: Aniridia-Wilms-tumor syndrome Hereditary disease: Nephrocalcinosis Hereditary disease: Dihydroxyadenin urolithiasis Hereditary disease: Glycolipidosis Hereditary disease: Diabetic nephropathy Hereditary disease: Donnai-Barrow syndrome Hereditary disease: Gitelman syndrome Hereditary disease: Apparent mineralocorticoid excess Hereditary disease: Arteriosclerosis Hereditary disease: Osteoporosis/renal Osteodystrophy Hereditary disease: MODY2 diabetes Hereditary disease: Methionine adenosyltransferase deficiency Hereditary disease: Inherited disorders of platelets Hereditary disease: Hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome Hereditary disease: Isolated growth hormone deficiency type 2 Hereditary disease: Juvenile onset glaucoma Hereditary disease: Alport Syndrome Hereditary disease: Mesangioproliferative glomerulonephritis Hereditary disease: Hemolytic-Uremic Syndrome Hereditary disease: Progressive osseous heteroplasia Hereditary disease: Disturbances of vitamin K metabolism Hereditary disease: Paroxysmal nocturnal hemoglobinuria Systematic index Hereditary disease: Thrombasthenia of Glanzmann and Naegeli Hereditary disease: MODY6 diabetes Hereditary disease: Albright hereditary osteodystrophy Hereditary disease: X-linked dominant hypophosphatemic rickets Hereditary disease: Hereditary Rickets Hereditary disease: Diabetic retinopathy Hereditary disease: Hyperinsulinemic hypoglycemia 6 Hereditary disease: Aminoaciduria Hereditary disease: Congenital nephrotic syndrome of the Finnish type Hereditary disease: Hereditary kidney diseases Hereditary disease: Pseudohypoaldosteronism type1 Hereditary disease: Fabry disease Hereditary disease: Hyperphosphaturia Hereditary disease: Thrombotic Thrombocytopenic Purpura Hereditary disease: Citrullinemia Hereditary disease: Isolated growth hormone deficiency type 1B Hereditary disease: Combined deficiency of vitamin K-dependent clotting factors type 2 Hereditary disease: Glomerulosclerosis 5 Hereditary disease: Hyperlipidemia Hereditary disease: Isolated growth hormone deficiency type 1A Hereditary disease: Congenital nephrotic syndrome, type 3 Hereditary disease: Hereditary glomerular disease Hereditary disease: Wilms tumor Hereditary disease: Hyperoxaluria Hereditary disease: MODY7 diabetes Hereditary disease: Hyperuricemic nephropathy, familial juvenile 1 Hereditary disease: Cystic kidney disease Hereditary disease: Transient neonatal diabetes mellitus 1 Hereditary disease: Hereditary bone disease Hereditary disease: Hereditary renal tumors Hereditary disease: Disorders of tubular solute transport Hereditary disease: Hyperoxaluria type I Hereditary disease: Medullary cystic kidney disease 2 Hereditary disease: EAST syndrome Hereditary disease: Neonatal diabetes mellitus Hereditary disease: Hyperuricemic nephropathy Hereditary disease: Pseudohypoparathyroidism Hereditary disease: Sialuria Hereditary disease: Hyperinsulinemic hypoglycemia 3 Hereditary disease: Nephrogenic diabetes insipidus Hereditary disease: Hypomagnesemia with secondary hypocalcemia Hereditary disease: Glomerulosclerosis 3 Hereditary disease: Nephronophthisis 2 Hereditary disease: Rabson-Mendenhall syndrome Hereditary disease: Fibrodysplasia ossificans progressiva Hereditary disease: Bronchiectasis with or without elevated sweat chloride 3 Hereditary disease: Isolated dominant hypomagnesemia Hereditary disease: Hereditary endocrinological diseases Hereditary disease: Nephronophthisis 1 Hereditary disease: Branchiootorenal dysplasia 1 Hereditary disease: Liddle syndrome Hereditary disease: Disturbances of glucose metabolism Hereditary disease: Infantile Bartter syndrome with deafness type 4 Hereditary disease: Interstitial kidney disease Hereditary disease: Fanconi-Bickel syndrome Hereditary disease: Nail-patella syndrome Hereditary disease: Lowe disease Hereditary disease: Growth hormone deficiency Hereditary disease: Bernard-Soulier syndrome Hereditary disease: Early-onset nephrotic syndrome with diffuse mesangial sclerosis Hereditary disease: Monogenic hypertension Hereditary disease: Hereditary metabolic kidney disease Hereditary disease: Classic Bartter syndrome Hereditary disease: Hereditary leiomyomatosis and renal cell cancer Hereditary disease: Cystinuria Hereditary disease: Vitamin D-dependent rickets, type 2A Hereditary disease: Schimke Immunoosseous dysplasia Hereditary disease: Antenatal Bartter syndrome type 1 Hereditary disease: Hypomagnesemia with hypercalciuria and nephrocalcinosis Hereditary disease: Branchiootorenal dysplasia 2 Hereditary disease: Histamine Intolerance Hereditary disease: Hereditary metabolic diseases Hereditary disease: Alloimmune thrombocytopenia Hereditary disease: Diabetes insipidus and mellitus with optic atrophy and deafness Hereditary disease: Hereditary pulmonary embolism Hereditary disease: Steroid-resistant nephrotic syndrome Hereditary disease: Pseudohypoaldosteronism type 2 Hereditary disease: Wolfram syndrome 2 Hereditary disease: Glomerulosclerosis Hereditary disease: Hereditary vascular disease Hereditary disease: Inherited human diseases of heterotopic bone formation Hereditary disease: Glomerulocystic kidney disease with hyperuricemia and isosthenuria Hereditary disease: Benign hyperproreninemia Hereditary disease: Hypertension Hereditary disease: Hereditary diabetes insipidus Hereditary disease: Glomerulosclerosis 2 Hereditary disease: Hypomagnesemia with normocalciuria Hereditary disease: Autosomal recessive hypophosphatemic rickets type 1 Hereditary disease: Kowarski syndrome Hereditary disease: Medullary cystic disease complex Hereditary disease: Hereditary Salt-wasting tubulopathies Hereditary disease: MODY3 diabetes Hereditary disease: Wolfram syndrome Hereditary disease: Urea cycle disorders Hereditary disease: Hyperparathyroidism Hereditary disease: MODY5 diabetes Hereditary disease: Frasier syndrome Hereditary disease: Vitamin D hydroxylation-deficient rickets type 1B Hereditary disease: MODY8 diabetes Hereditary disease: Hereditary neurological disorders Hereditary disease: Renal tubular acidosis type 3 with osteopetrosis Hereditary disease: Hypoparathyroidism Hereditary disease: Nephrolithiasis diarrhea syndrome Hereditary disease: Monosacchariduria Hereditary disease: Thrombotic microangiopathies Hereditary disease: Nephrotic syndrome Hereditary disease: Permanent neonatal diabetes mellitus Hereditary disease: Citrullinemia type 1 Hereditary disease: Lysinuric protein intolerance Hereditary disease: HADH deficiency Hereditary disease: Thromboembolic diseases Hereditary disease: Hypomagnesemia with hypercalciuria and nephrocalcinosis with ocular involvement Hereditary disease: Hereditary bleeding disorders Hereditary disease: Autosomal dominant polycystic kidney disease Hereditary disease: Leprechaunism Hereditary disease: Alström syndrome Hereditary disease: Diabetes mellitus Hereditary disease: Infantile sialic acid storage disorder Hereditary disease: Lysosomal storage disease Hereditary disease: Autosomal recessive polycystic kidney and hepatic disease 1 Welcome to IvanPeters.com Hereditary disease: Hereditary disease: Isolated growth hormone deficiency type 3 Hereditary disease: Pseudohypoaldosteronism Hereditary disease: Citrullinemia Hereditary disease: Denys-Drash syndrome Hereditary disease: Hereditary diseases of the hematopoetic system and coagulopathies Hereditary disease: Bartter syndrome Hereditary disease: Hyperuricemic nephropathy, familial juvenile 2 Hereditary disease: Transient neonatal diabetes mellitus 3 Hereditary disease: Membranoproliferative glomerulonephritis Hereditary disease: Nonaka myopathy Hereditary disease: MODY9 diabetes Hereditary disease: Salla disease Hereditary disease: Nephronophthisis 4 Hereditary disease: Vitamin D-dependent rickets, type 2B Hereditary disease: MODY1 diabetes Hereditary disease: Glucose-Galactose Malabsorption Hereditary disease: Hyperinsulinemic hypoglycemia 1 Hereditary disease: Nephritic syndrome Hereditary disease: Ovalocytosis Hereditary disease: Nephronophthisis 6 Hereditary disease: Developmental delay, epilepsy, and neonatal diabetes Hereditary disease: MODY diabetes Hereditary disease: Nephronophthisis Hereditary disease: Coumarin resistance Hereditary disease: Renal Glucosuria Hereditary disease: Antenatal Bartter syndrome type 2 Hereditary disease: Alzheimer disease Hereditary disease: Cystinosis Hereditary disease: Hyperinsulinemic hypoglycemia 4 Hereditary disease: Hypomagnesemia Hereditary disease: Bronchiectasis with or without elevated sweat chloride 2 Hereditary disease: Renal Hypouricemia Hereditary disease: Hyperinsulinemic hypoglycemia 5 Hereditary disease: Epstein syndrome Hereditary disease: Dent disease Hereditary disease: Bardet-Biedel syndrome Hereditary disease: Bardet-Biedl syndrome Hereditary disease: Hereditary ocular disease and visual impairment Hereditary disease: Renal tubular dysgenesis Hereditary disease: Bronchiectasis with or without elevated sweat chloride Hereditary disease: Hyperoxaluria type II Hereditary disease: Osteopetrosis Hereditary disease: Hemochromatosis Hereditary disease: MODY10 diabetes Hereditary disease: Autosomal recessive hypophosphatemic rickets type 2 Hereditary disease: Renal cysts and diabetes (RCAD) Hereditary disease: Urolithiasis Hereditary disease: Renal tubular acidosis Hereditary disease: Hereditary broncho-pulmonary disease Hereditary disease: Pseudohypoparathyroidism type IB Hereditary disease: Glomerulonephritis Hereditary disease: HIV resistance Hereditary disease: Glomerulosclerosis 1 Hereditary disease: Congenital abnormalities of the kidney and urinary tract Hereditary disease: Vitamin D hydroxylation-deficient rickets type 1A Hereditary disease: Wolfram syndrome 1 Hereditary disease: WAGR syndrome Hereditary disease: Branchiootorenal dysplasia Hereditary disease: Glucocorticoid-remediable aldosteronism Hereditary disease: Hyperinsulinemic hypoglycemia Hereditary disease: MODY4 diabetes Hereditary disease: Combined deficiency of vitamin K-dependent clotting factors type 1 Hereditary disease: Lesch-Nyhan syndrome Hereditary disease: Glomerulosclerosis 4 Hereditary disease: Transient neonatal diabetes mellitus 2 Hereditary disease: Nephronophthisis 3 Hereditary disease: Kelley-Seegmiller syndrome Hereditary disease: Hyperinsulinemic hypoglycemia 2 Hereditary disease: MYH9 related disorders Hereditary disease: Renal-hepatic-pancreatic dysplasia Hereditary disease: Central diabetes insipidus Hereditary disease: Autosomal dominant hypophosphatemic rickets research Research Test status: research versus clinical test mail Contact information Web mail form Thank you sample Sample requirements Copyright © 2005-2011 by Center for Nephrology and Metabolic Disorders Dr. Mato Nagel, MD Albert-Schweitzer-Ring 32, D-02943 Weisswasser Tel.: +49-3576-287922, Fax: +49-3576-287944 Sitemap | e-mail | All rights reserved. | Data protection