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A
ADH resistance
Adolescent nephronophthisis
Albright hereditary osteodystrophy
Aldosteronism With Normal Blood Pressure
Alloimmune thrombocytopenia
Alport syndrome with macrothrombocytopenia
Alport Syndrome
Alström syndrome
Alzheimer disease
Alzheimer disease
Aminoaciduria
Anderson-Fabry disease
Angiokeratoma diffusum
Antenatal Bartter syndrome type 1
Antenatal Bartter syndrome type 2
Apparent mineralocorticoid excess, type 1
Apparent mineralocorticoid excess, type 2
Apparent mineralocorticoid excess
APRT deficiency
Arteriosclerosis
Arteriosclerotic vascular disease
Arthro-osteo-onychodysplasia
Atherosclerosis,arteriosclerosis
Atherosclerotic vascular disease
Autosomal dominant diabetes mellitus
Autosomal dominant hypophosphatemic rickets
Autosomal dominant polycystic kidney disease
Autosomal recessive polycystic kidney and hepatic disease 1
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
B
Bardet-Biedel syndrome
Bartter syndrome type 1
Bartter syndrome type 2
Bartter syndrome type 4
Bartter syndrome, classic
Bartter syndrome
Benign hyperproreninemia
Bernard-Soulier syndrome
Bilateral macular coloboma with hypercalciuria
Bladder stones, hereditary
Blood pressure, elevated
Branchiootorenal dysplasia 1
Branchiootorenal dysplasia 2
Branchiootorenal dysplasia
Branchiootorenal syndrome 1
Branchiootorenal syndrome 2
Branchiootorenal syndrome
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
C
Calcium containing kidney stones
Central diabetes insipidus
Citrullinemia
Citrullinemia
Citrullinemia type 1
Classic Bartter syndrome
Cochleosaccular degeneration
Complete hypoxanthine guanine phosphoribosyltransferase 1 deficiency
Congenital abnormalities of the kidney and urinary tract
Congenital hepatic fibrosis
Congenital nephrosis
Congenital nephrotic syndrome 1
Congenital nephrotic syndrome of the Finnish type
Congenital nephrotic syndrome, type 3
Cortisol 11-beta-ketoreductase deficiency
Cystic kidney disease
Cystinuria
Cystinuria
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
D
Deafness, autosomal dominant nonsyndromic sensorineural 17
Deafness, autosomal dominant nonsyndromic sensorineural 17
Deficient gamma-carboxylation of glutamic acid
Dent disease
Denys-Drash syndrome
Developmental delay, epilepsy, and neonatal diabetes
Diabetes insipidus
Diabetes mellitus
Diabetes mellitus
Diabetic eye disease
Diabetic kidney disease
Diabetic nephropathy
Diabetic nephropathy
Diabetic retinopathy
Diabetic retinopathy
Diffuse mesangial sclerosis
Dihydroxyadenin urolithiasis
Disease progression in diabetic nephropathy
Disorders of tubular solute transport
Distal tubular acidosis
Disturbances in magnesium balance
Disturbances of glucose metabolism
Disturbances of vitamin K metabolism
Dmrv
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
E
Early-onset hyperuricemia, anemia, and progressive kidney failure
Early-onset nephrotic syndrome with diffuse mesangial sclerosis
Endocrinological disorders caused by hereditary kidney disease
Epstein syndrome
Epstein syndrome
Errors of metabolism
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
F
Fabry disease
Factors II, VII, IX, and X, combined deficiency
Familial diabetes (MODY1)
Familial diabetes (MODY10)
Familial diabetes (MODY2)
Familial diabetes (MODY3)
Familial diabetes (MODY4)
Familial diabetes (MODY5)
Familial diabetes (MODY6)
Familial diabetes (MODY7)
Familial diabetes (MODY8)
Familial diabetes (MODY9)
Familial diabetes insipidus
Familial diabetes mellitus:risk for diabetic complications
Familial diabetes mellitus
Familial glaucoma
Familial hemolytic uremic syndrome
Familial HUS
Familial hyperinsulinemic hypoglycemia
Familial hyperinsulinism
Familial hyperkalemia and hypertension, Gordon syndrome
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis with ocular involvement
Familial hypomagnesemia with hypercalciuria and nephrocalcinosis
Familial juvenile hyperuricemic nephropathy 1
Familial juvenile nephronophthisis
Familial multiple coagulation factor deficiency III
Fanconi-Bickel syndrome
Fechtner syndrome
Finnish type sialuria
Focal and segmental glomerulosclerosis 1
Focal and segmental glomerulosclerosis 2
Focal and segmental glomerulosclerosis 3
Focal and segmental glomerulosclerosis
Fong disease
Fragility fractures
Frasier syndrome
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
G
Giant platelet syndrome
Gitelman syndrome
Glanzmann thrombasthenia
Glaucoma
Glomerulocystic kidney disease with hyperuricemia and isosthenuria
Glomerulonephritis (IgA nephropathy)
Glomerulosclerosis 1
Glomerulosclerosis 2
Glomerulosclerosis 3
Glomerulosclerosis 4
Glomerulosclerosis 5
Glomerulosclerosis
Glucocorticoid-remediable aldosteronism
Glucose-Galactose Malabsorption
Glycogenosis, fanconi type
Glycolipidosis
Goldston syndrome
Growth hormone deficiency
Guibaud-Vainsel syndrome
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
H
Haemolytic uremic syndrome
Hemochromatosis
Hemolytic uremic syndrome
Hemolytic-Uremic Syndrome
Hepatorenal glycogenosis with renal Fanconi syndrome
Hereditary bladder stones
Hereditary bleeding disorders
Hereditary bone disease
Hereditary diabetes (MODY1)
Hereditary diabetes (MODY10)
Hereditary diabetes (MODY2)
Hereditary diabetes (MODY3)
Hereditary diabetes (MODY4)
Hereditary diabetes (MODY5)
Hereditary diabetes (MODY6)
Hereditary diabetes (MODY7)
Hereditary diabetes (MODY8)
Hereditary diabetes (MODY9)
Hereditary diabetes insipidus
Hereditary diabetes mellitus
Hereditary diabetes mellitus
Hereditary diseases of the hematopoetic system and coagulopathies
Hereditary disturbances in solute transport
Hereditary dystopic lipidosis
Hereditary endocrinological diseases
Hereditary glaucoma
Hereditary glomerular disease
Hereditary hemolytic uremic syndrome
Hereditary HUS
Hereditary hypomagnesemia with hypercalciuria and nephrocalcinosis and severe ocular involvement
Hereditary hypomagnesemia with hypercalciuria and nephrocalcinosis
Hereditary kidney diseases
Hereditary kidney stones
Hereditary leiomyomatosis and renal cell cancer
Hereditary leiomyomatosis and renal cell cancer
Hereditary metabolic diseases
Hereditary metabolic kidney disease
Hereditary multiple leiomyoma of skin
Hereditary nephritis
Hereditary nephrolithiasis
Hereditary neurological disorders
Hereditary ocular disease and visual impairment
Hereditary proteinuria syndromes
Hereditary renal malformations
Hereditary renal tumors
Hereditary rickets
Hereditary Salt-wasting tubulopathies
Hereditary thrombotic thrombocytopenic purpura
Hereditary tubular dysfunction
Hereditary tumors
Hereditary urolithiasis
Hereditary vascular disease
HIV resistance
HPRT deficiency, complete
HPRT deficiency, partial
Hyperaldosteronism With Hypokalemic Alkalosis
Hyperaldosteronism Without Hypertension
Hyperaldosteronism, familial, type i
Hyperinsulinemic hypoglycemia 1
Hyperinsulinemic hypoglycemia 2
Hyperinsulinemic hypoglycemia 3
Hyperinsulinemic hypoglycemia 4
Hyperinsulinemic hypoglycemia 5
Hyperinsulinemic hypoglycemia 6
Hyperinsulinemic hypoglycemia
Hyperlipidemia
Hyperoxaluria
Hyperoxaluria type I
Hyperoxaluria type II
Hyperparathyroidism
Hyperphosphaturia
Hyperphosphaturia
Hyperproreninemia
Hypertension
Hypertension, monogenic
Hyperuricemic nephropathy, familial juvenile 1
Hyperuricemic nephropathy, familial juvenile 2
Hyperuricemic nephropathy
Hypokalemic Alkalosis with Hypercalciuria
Hypokalemic alkalosis with hypercalciuria, antenatal, 2
Hypokalemic salt-losing tubulopathy
Hypomagnesaemia
Hypomagnesemia 2
Hypomagnesemia
Hypomagnesemia
Hypomagnesemia with hypercalciuria and nephrocalcinosis with ocular involvement
Hypomagnesemia with hypercalciuria and nephrocalcinosis
Hypomagnesemia with normocalciuria
Hypomagnesemia with secondary hypocalcemia
Hypomagnesemia-hypokalemia, primary renotubular, with hypocalciuria
Hypomagnesemic tetany
Hypoparathyroidism
Hypophosphatemia
Hypophosphatemia, x-linked
Hypophosphatemic x-linked vitamin D-resistant rickets
Hypothalamic diabetes insipidus
Hypouricemia, renal
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
I
Idiopathic nephrotic syndrome
Immunoosseous dysplasia of the Schimke type
Inclusion body myopathy 2
Infantile Bartter syndrome with deafness type 4
Infantile nephronophthisis
Infantile sialic acid storage disorder
Inherited disorders of platelets
Inherited thrombophilia
Interstitial kidney disease
Intestinal hypomagnesemia with secondary hypocalcemia
Isolated dominant hypomagnesemia
Isolated growth hormone deficiency, type ii
Isolated recessive hypomagnesemia
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
J
Juvenil onset glaucoma
Juvenile nephronophthisis 4
Juvenile onset glaucoma
Juxtaglomerular Hyperplasia
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
K
Kelley-Seegmiller syndrome
Kidney disease appearing as endocrinological disorders
Kidney disease in diabetes mellitus
Kidney stones of cystine
Kidney stones, hereditary
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
L
Lesch-Nyhan syndrome
Liddle syndrome
Lowe disease
Lowe oculocerebrorenal syndrome
Lowe syndrome
Lysinuric protein intolerance
Lysosomal storage disease
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
M
Macrothrombocytopenia and progressive sensorineural deafness
Magnesium deficiency
Magnesium wastage
Marble bones
MAT deficiency
Maturity onset diabetes of the young type 1 (MODY1)
Maturity onset diabetes of the young type 2 (MODY2)
Maturity onset diabetes of the young type 3 (MODY3)
Maturity onset diabetes of the young type 4 (MODY4)
Maturity onset diabetes of the young type 5 (MODY5)
Maturity onset diabetes of the young type 6 (MODY6)
Maturity onset diabetes of the young type 7 (MODY7)
Maturity onset diabetes of the young type 8 (MODY8)
Maturity onset diabetes of the young type 9 (MODY10)
Maturity onset diabetes of the young type 9 (MODY9)
Maturity onset diabetes of the young
May-Hegglin anomaly
May-Hegglin anomaly
Meckel-like syndrome
Medullary cystic disease complex
Medullary cystic kidney disease 2
Medullary sponge kidney
Melnick-Fraser syndrome
Mesangial sclerosis
Metabolic disease with renal symptoms
Methionine adenosyltransferase deficiency
Microcoria-congenital nephrotic syndrome
Mixed proximal-distal renal tubular acidosis
MODY diabetes
MODY1 diabetes
MODY10 diabetes
MODY2 diabetes
MODY3 diabetes
MODY4 diabetes
MODY5 diabetes
MODY6 diabetes
MODY7 diabetes
MODY8 diabetes
MODY9 diabetes
Monogenic hypertension
Monosacchariduria
Multiple coagulation factor deficiency III
MYH9 related disorders
Myopathy, distal, with rimmed vacuoles
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
N
Nail-patella syndrome
Neonatal diabetes mellitus
Nephritic syndrome
Nephritis
Nephroblastoma
Nephrocalcinosis
Nephrogenic diabetes insipidus
Nephrolithiais, hereditary
Nephronophthisis 1
Nephronophthisis 2
Nephronophthisis 3
Nephronophthisis 4
Nephronophthisis 6
Nephronophthisis
Nephropathy, familial, with gout
Nephrosialidosis
Nephrotic syndrome
Neurogenic diabetes insipidus
Nonaka distal myopathy
Nonaka myopathy
Normocalciuric renal hypomagnesemia
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
O
Onychoosteodysplasia
Open angle glaucoma
Osteo-onychodystrophy with nephropathy
Osteopetrosis
Osteoporosis
Osteoporosis/renal Osteodystrophy
Osteoporosis
Oxalosis
Oxalosis I
Oxalosis II
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
P
Partial hypoxanthine guanine phosphoribosyltransferase 1 deficiency
Pentosuria
Permanent neonatal diabetes mellitus
Pierson syndrome
Pituitary dwarfism due to isolated growth hormone deficiency, autosomal dominant
Polycystic kidneys
Predisposition of hypertension
Proximal renal tubular acidosis
Pseudohyperaldosteronism
Pseudohypoaldosteronism
Pseudohypoaldosteronism type 2
Pseudohypoaldosteronism type1
Pseudohypoparathyroidism
Pseudohypoparathyroidism type IA
Pseudohypoparathyroidism type IB
Pseudovitamin D deficiency
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
R
Renal cysts and diabetes (RCAD)
Renal cysts and diabetes (RCAD)
Renal Glucosuria
Renal hypomagnesemia with normocalciuria, Hypomagnesemia 4
Renal Hypouricemia
Renal magnesium loss
Renal Osteodystrophy
Renal resistance to PTH
Renal tubular acidosis type 3 with osteopetrosis
Renal tubular acidosis
Renal tubular acidosis
Renal tubular dysgenesis
Renal-hepatic-pancreatic dysplasia with Dandy-Walker cyst
Renal-hepatic-pancreatic dysplasia
Renale hypomagnesemia 2
Rickets
Rickets
Risk of arteriosclerosis
Risk of atherosclerosis
Risk of diabetic nephropathy
Risk of diabetic retinopathy
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
S
Salla disease
Salt-losing tubulopathy, hereditary
Schimke Immunoosseous dysplasia
Schulman-Upshaw syndrome
Sebastian syndrome
Sebastian syndrome
Sialuria
Sialuria French type
Solute transport disturbances
Steroid-resistant nephrotic syndrome
Syndromes of salt wastage
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
T
Thiazide-like salt-losing tubulopathy
Thrombasthenia of Glanzmann and Naegeli
Thromboembolic diseases
Thrombophilia
Thrombotic microangiopathies
Thrombotic microangiopathies
Thrombotic thrombocytopenic purpura
Thrombotic Thrombocytopenic Purpura
Transient neonatal diabetes mellitus 1
Transient neonatal diabetes mellitus 2
Transient neonatal diabetes mellitus 3
Tubular disorders
Tubular kidney diseases
Tubulopathies, hereditary
Turner-Kieser syndrome
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
U
Upshaw-Schulman syndrome
Urea cycle disorders
Uremic medullary cystic disease
Uric acid nephrolithiasis, Uric acid kidney stones
Uric acid nephropathy
Urolithiasis
Urolithiasis, hereditary
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
V
Vasopressin resistance
Vitamin D-resistant rickets, x-linked
Vitamin D-resistent rickets, autosomal dominant
Vitamin K-dependent coagulation defect
Von Willebrand factor receptor deficiency
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
W
WAGR syndrome
Wilms tumor
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
X
X-linked dominant hypophosphatemic rickets
X-linked recessive nephrolithiasis
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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