SE-ATLAS

Syndrome d'amélogenèse imparfaite-néphrocalcinose Acidose tubulaire rénale proximale autosomique dominante Syndrome de Joubert avec atteinte oculo-rénale Syndrome de Liddle Syndrome de Galloway-Mowat Syndrome d'Imerslund-Gräsbeck Syndrome oculo-cérébro-rénal de Lowe Lupus érythémateux systémique Ectasie canaliculaire précalicielle Sclérose tubéreuse de Bourneville Syndrome nail-patella Dysplasie rénale multikystique Agénésie rénale Sténose congénitale de l'artère rénale Syndrome d'Alport Syndrome d'Alström Excès apparent de minéralocorticoïdes Glomérulonéphrite membranoproliférative primaire Néphropathie tubulo-intersitielle autosomique dominante Hyperaldostéronisme familial type IV Syndrome de néphronophtise familiale de l'adulte-quadriparésie spastique Néphrite tubulo-interstitielle et uvéite Syndrome de Bardet-Biedl Syndrome de Pierson Syndrome de Senior-Boichis Néphropathie tubulo-intersitielle autosomique dominante associée à MUC1 Néphropathie tubulo-interstitielle autosomique dominante associée à UMOD Acidémie méthylmalonique résistante à la vitamine B12 type mut0 Syndrome de Birt-Hogg-Dubé Glomérulopathie à dépôts de fibronectine Maladie de von Hippel-Lindau Acidose tubulaire rénale distale autosomique récessive Anomalie congénitale de la glycosylation avec une néphropathie comme manifestation majeure Hyperaldostéronisme familial type III Congenital thrombotic thrombocytopenic purpura Immune-mediated thrombotic thrombocytopenic purpura Familial hyperaldosteronism type I Familial hyperaldosteronism type II Idiopathic hypercalciuria Severe oculo-renal-cerebellar syndrome Primary hyperoxaluria type 1 Primary hyperoxaluria type 3 Bartter syndrome type 3 Hypertrophic cardiomyopathy with kidney anomalies due to mitochondrial DNA mutation Immunoglobulin-mediated membranoproliferative glomerulonephritis Cystinuria type B Renal hypoplasia Bartter syndrome type 1 Autosomal dominant polycystic kidney disease Denys-Drash syndrome Atypical hemolytic uremic syndrome with anti-factor H antibodies Hereditary pheochromocytoma-paraganglioma Genetic steroid-resistant nephrotic syndrome Late-onset nephronophthisis Hemolytic uremic syndrome with DGKE deficiency Juvenile nephronophthisis Primary hyperoxaluria type 2 Collecting duct carcinoma Fetal lower urinary tract obstruction Autosomal recessive proximal renal tubular acidosis Autosomal dominant distal renal tubular acidosis Saldino-Mainzer syndrome EAST syndrome Cystinuria type A RHYNS syndrome Methylmalonic acidemia with homocystinuria, type cblC Renal dysplasia Bartter syndrome type 2 HNF1B-related autosomal dominant tubulointerstitial kidney disease Dent disease type 2 Hypotonia-cystinuria type 1 syndrome Dent disease type 1 Autosomal dominant intermediate Charcot-Marie-Tooth disease type E C3 glomerulopathy Hemolytic uremic syndrome Hereditary papillary renal cell carcinoma Atypical hemolytic uremic syndrome with complement gene abnormality Vitamin B12-unresponsive methylmalonic acidemia type mut- Cystinosis Familial steroid-resistant nephrotic syndrome with adrenal insufficiency Autosomal recessive polycystic kidney disease Gitelman syndrome Hereditary leiomyomatosis and renal cell cancer Familial vesicoureteral reflux Joubert syndrome with renal defect Senior-Loken syndrome Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis Primary Fanconi renotubular syndrome Bartter syndrome type 5 Fabry disease Bartter syndrome type 4 Hypertension due to gain-of-function mutations in the mineralocorticoid receptor Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation Frasier syndrome Hypoxanthine guanine phosphoribosyltransferase partial deficiency Nephrogenic diabetes insipidus REN-related autosomal dominant tubulointerstitial kidney disease Juvenile cataract-microcornea-renal glucosuria syndrome Pseudohypoaldosteronism type 2 Brachydactyly-arterial hypertension syndrome Lesch-Nyhan syndrome