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AA amyloidosis AApoAI amyloidosis AApoAII amyloidosis AApoAIV amyloidosis Acquired thrombotic thrombocytopenic purpura (TTP)Acro-pectoro-renal dysplasia Acroosteolysis dominant type Acrorenal syndrome Action myoclonus-renal failure syndrome Adenine phosphoribosyltransferase deficiency Adult-onset Still disease AFib amyloidosis AH amyloidosis AL amyloidosis Alagille syndrome Alport syndrome Alport syndrome, autosomal dominant Alport syndrome, autosomal recessive Alport syndrome, digenic Alport syndrome, X-linked Alport syndrome, X-linked with diffuse leiomyomatosis Alström Syndrome ALys amyloidosis Amelogenesis imperfecta-nephrocalcinosis syndrome Aniridia-renal agenesis-psychomotor retardation syndrome Anterior urethral valve Anti-glomerular basement membrane disease Apparent mineralocorticoid excess AREDYLD (acral-renal-ectodermal-dysplasia-lipoatrophic-diabetes) syndrome Arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome Atresia of urethra Atypical hemolytic uremic syndrome (aHUS)Atypical hemolytic uremic syndrome (aHUS) due to Methylcobalamin deficiency, type CblC Atypical hemolytic uremic syndrome (aHUS) with anti-factor H antibodies Atypical hemolytic uremic syndrome (aHUS) with complement gene abnormality Atypical hemolytic uremic syndrome (aHUS) with DGKE deficiency Atypical hemolytic uremic syndrome (aHUS), not further specified Auto-immune distal renal tubular acidosis Autoimmune hepatitis Autoimmune interstitial lung disease-arthritis syndrome Autosomal dominant polycystic kidney disease (ADPKD)Autosomal dominant distal renal tubular acidosis (dRTA)Autosomal dominant hypocalcemia Autosomal dominant hypophosphatemic rickets Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (ADPKD-TSC)Autosomal dominant primary hypomagnesemia with hypocalciuria Autosomal dominant proximal renal tubular acidosis Autosomal dominant tubulointerstitial kidney disease (ADTKD)Autosomal recessive distal renal tubular acidosis (dRTA)Autosomal recessive hypophosphatemic rickets Autosomal recessive infantile hypercalcemia Autosomal recessive polycystic kidney disease (ARPKD)Autosomal recessive proximal renal tubular acidosis Bardet-Biedl syndrome Bardet-Biedl syndrome (renal / urinary tract malformation)Bartter syndrome Beckwith-Wiedemann syndrome Beh Bilateral multicystic dysplastic kidney Bladder exstrophy BNAR (Bifid nose, anorectal and renal anomalies) syndrome BOR (branchio-oto-renal) syndrome Brachydactyly-arterial hypertension syndrome Buerger disease C3 glomerulonephritis C3 glomerulopathy C3 glomerulopathy secondary to MGRS Cat-eye syndrome Caudal regression sequence Cerebrorenodigital (Meckel-like) syndrome CHARGE syndrome Childhood-onset systemic lupus erythematosus (SLE)Childhood-onset systemic lupus erythematosus associated TMA (SLE)Cloacal exstrophy Collagen type III glomerulopathy Collagenopathies (inc. Alport syndrome)Collagenopathy, not further specified Congenital hydronephrosis Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization Congenital nephrotic syndrome, Finnish type Congenital nephrotic syndrome, no genetic cause specified Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome Congenital primary megaureter Congenital primary megaureter, nonrefluxing and unobstructed form Congenital primary megaureter, obstructed form Congenital primary megaureter, refluxing and obstructed Congenital primary megaureter, refluxing form Congenital thrombotic thrombocytopenic purpura (TTP)Cornelia de Lange syndrome Cranioectodermal dysplasia (Sensenbrenner syndrome)CREST syndrome Cryoglobulinemic vasculitis Cystinuria De novo thrombotic microangiopathy after kidney transplantation Dense deposit disease Dent disease Dent disease type 1 (CLCN5-related)Dent disease type 2 (OCRL-related)Denys-Drash syndrome Dermatomyositis Di George syndrome (22q11.2 deletion)Diffuse cutaneous systemic sclerosis Distal renal tubular acidosis Distal renal tubular acidosis with hemolytic anemia Donnai-Barrow syndrome Drug-related renal tubular dysgenesis EAST syndrome EEC (Ectrodactyly-ectodermal dysplasia-cleft lip/palate) syndrome Ellis van Creveld syndrome Eosinophilic granulomatosis with polyangiitis Epispadias Exstrophy-epispadias complex Fabry disease Faconi syndrome, induced by other heavy metal Familial hyperaldosteronism Familial hyperaldosteronism type I (glucocorticoid-sensitive hypertension)Familial hyperaldosteronism type II Familial hyperaldosteronism type III Familial Mediterranean fever Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement Familial primary hypomagnesemia with hypocalcuria Familial primary hypomagnesemia with normocalciuria and normocalcemia Familial renal glucosuria Familial steroid-resistant nephrotic syndrome with adrenal insufficiency Fanconi syndrome, Cisplatin induced Fanconi syndrome, drug induced Fanconi syndrome, heavy metal induced Fanconi syndrome, induced by other drug Fanconi syndrome, lead induced Fanconi syndrome, mercury induced Fanconi syndrome, monoclonal Ig light chain-associated Fanconi syndrome, primary Fetal lower urinary tract obstruction (LUTO)Fibronectin glomerulopathy Fraser syndrome Frasier syndrome Galactosemia Galloway-Mowat syndrome Generalized pseudohypoaldosteronism type 1 Genetic hypertension involving tubular dysfunction Genetic primary hypomagnesemia Genetic primary hypomagnesemia with normocalcuria Genetic steroid-resistant nephrotic syndrome (SRNS)Giant cell arteritis Gitelman syndrome Gitelman-like syndrome Glomerulopathy as part of a genetic systemic disease Glomerulopathy as part of a non-genetic systemic disease Glomerulopathy as part of a syndromic disorder Glomerulopathy as part of a systemic disorder Glycogen storage disease due to glucose-6-phosphatase deficiency Glycogen storage disease due to GLUT2 deficiency Granulomatosis with polyangiitis (Wegener)HANAC syndrome HDR (Hypoparathyroidism-deafness-renal disease) syndrome Heavy chain deposition disease Hemolytic uremic syndrome (HUS)Hereditary amyloidosis with primary renal involement Hereditary hypophosphatemic rickets with hypercalciuria Hereditary renal hypouricemia Hereditary xanthinuria HNF1B-related autosomal dominant tubulointerstitial kidney disease (ADTKD)Holoprosencephaly-radial heart renal anomalies syndrome Hypercalciuria, idiopathic Hypocomplementemic urticarial vasculitis Hypokalemic alkalosis, CLDN10 associated Hypomagnesaemia, drug-induced Hypophosphatemia, dominant, with nephrolithiasis or osteoporosis Hypophosphatemic rickets Hypotonia-cystinuria syndrome Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome Hypoxanthine-guanine phosphoribosyltransferase deficiency Idiopathic multidrug-resistant nephrotic syndrome Idiopathic non-lupus full-house nephropathy Idiopathic steroid-resistant nephrotic syndrome Idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunouppressive therapy Idiopathic steroid-sensitive nephrotic syndrome Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance IgA nephropathy IgG4-related kidney disease Imerslund-Gräsbeck syndrome Immunoglobulin A vasculitis (Henoch Schonlein nephritis, PSH)Immunoglobulin-mediated membranoproliferative glomerulonephritis (MPGN)Immunotactoid glomerulopathy Immunotactoid or fibrillary glomerulopathy Infantile nephronophthisis Infantile nephropathic cystinosis Infection-related hemolytic uremic syndrome (HUS)Infundibulopelvic stenosis-multicystic kidney syndrome Isolated autosomal dominant hypomagnesemia, Glaudemans type Jeune syndrome (ciliopathies)Jeune syndrome (renal / urinary tract malformation)Joubert syndrome with oculorenal defect Joubert syndrome with renal defect Juvenile dermatomyositis Juvenile nephronophthisis Juvenile nephropathic cystinosis Juvenile polymyositis Kabuki Syndrome Kallmann syndrome Karyomegalic interstitial nephritis Late-onset nephronophthisis LCAT deficiency Leigh syndrome with nephrotic syndrome Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome Liddle Syndrome Light and heavy chain deposition disease Light chain deposition disease Limited cutaneous systemic sclerosis Limited systemic sclerosis Lipoprotein glomerulopathy Lowe syndrome Lysinuric protein intolerance Mayer-Rokitansky-K Meckel syndrome (ciliopathies)Meckel syndrome (renal / urinary tract malformation)Medullary sponge kidney Megacystis-megaureter syndrome Megacystis-microcolon-intestinal hypoperistalsis syndrome Membranous glomerulonephritis Methylmalonic acidemia (without homocystinuria)Methylmalonic acidemia, Vitamin B12-responsive Methylmalonic acidemia, Vitamin B12-unresponsive Microscopic (including familial) hematuria Microscopic polyangiitis Mixed connective tissue disease Monoclonal gammopathy of renal significance (MGRS)MUC1-related autosomal dominant tubulointerstitial kidney disease (ADTKD)Muckle-Wells syndrome Multicentric carpo-tarsal osteolysis with or without nephropathy Multicystic dysplastic kidney MYH9-related disease Nail-patella syndrome Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome Nephrogenic diabetes insipidus Nephrogenic syndrome of inappropriate antidiuresis Nephronophthisis Nephropathic cystinosis Nephrotic syndrome without extrarenal manifestations Nephrotic syndrome, familial, steroid-resistant (SRNS), with sensorineural deafness Nephrotic syndrome, genetic Nephrotic syndrome, idiopathic Nephrotic syndrome, syndromic, not otherwise specified Nephrotic syndrome-deafness-pretibial epidermolysis bullosa syndrome Neurofibromatosis type 1 Neurogenic bladder, congenital or acquired Non-amyloid fibrillary glomerulopathy Non-amyloid monoclonal immunoglobulin deposition disease Non-syndromic renal or urinary tract malformation Noonan syndrome Ochoa syndrome OFD (Orofaciodigital) syndrome type 1 Oligomeganephronia Oncogenic osteomalacia Osteopetrosis with renal tubular acidosis Other autoimmune dRTA Pallister-Hall syndrome Pauci-immune glomerulonephritis Pauci-immune glomerulonephritis with ANCA Pauci-immune glomerulonephritis without ANCA Phosphoribosylpyrophosphate synthetase superactivity Pierson syndrome Polyarteritis nodosa Polymyositis Posterior urethral valve (PUV)Primary biliary cholangitis Primary hyperoxaluria Primary hyperoxaluria type 1 (PH1)Primary hyperoxaluria type 2 (PH2)Primary hyperoxaluria type 3 (PH3)Primary hypomagnesemia with refractory seizures and intellectual disability Primary hypomagnesemia with secondary hypocalcemia Primary localized amyloidosis Primary megaureter, adult-onset form Primary membranoproliferative glomerulonephritis (MPGN)Primary renal tubular acidosis Primary systemic amyloidosis Proliferative glomerulonephritis with monoclonal immune deposits (PGNMID)Proximal renal tubular acidosis Prune belly syndrome Pseudohypoaldosteronism type 1 Pseudohypoaldosteronism type 2 RCAD (Renal cysts and diabetes) syndrome Relapsing polychondritis REN-related autosomal dominant tubulointerstitial kidney disease (ADTKD, FJHN type 1)Renal agenesis Renal agenesis, bilateral Renal agenesis, unilateral Renal artery stenosis, congenital Renal coloboma syndrome Renal dysplasia Renal dysplasia, bilateral Renal dysplasia, unilateral Renal hypoplasia Renal hypoplasia, bilateral Renal hypoplasia, unilateral Renal nutcracker syndrome Renal pseudohypoaldosteronism type 1 Renal tubular dysgenesis Renal tubular dysgenesis due to twin-twin transfusion Renal tubular dysgenesis of genetic origin Renal-hepatic-pancreatic dysplasia Reynolds syndrome RHYNS (retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysaplasia) syndrome Rubinstein-Taybi syndrome Saldino-Mainzer (conorenal) syndrome Sarcoidosis Schimke immuno-osseous dysplasia Schinzel-Giedion syndrome Senior-Boichis syndrome Senior-Loken syndrome SERKAL syndrome Severe oculo-renal-cerebellar syndrome Shiga toxin-associated hemolytic uremic syndrome (STEC-HUS)Simpson-Golabi-Behmel syndrome Sjogren Syndrome Smith-Lemli-Opitz syndrome Streptoccous pneumoniae-associated hemolytic uremic syndrome (HUS) Syndromic renal or urinary tract malformation Systemic Lupus Erythematosus (SLE)Systemic Lupus Erythematosus associated TMA (SLE)Systemic sclerosis Systemic vasculitis associated with glomerulopathy Takayasu arteritis Thrombotic thrombocytopenic purpura (TTP)Thyrocerebrorenal syndrome Townes-Brocks syndrome Trisomy 13 Trisomy 18 Tuberous sclerosis complex (TSC)Tubulointerstitial nephritis and uveitis syndrome Tubulopathy due to mitochondrial oxidative phosphorylation disorder Turner syndrome UMOD-related autosomal dominant tubulointerstitial kidney disease (ADTKD)Unilateral multicystic dysplastic kidney Ureteropelvic junction (UPJ) obstruction (bilateral or in solitary kidney)VACTERL/VATER association Vesicoureteric reflux (VUR), familial Vesicoureteric reflux (VUR), high-grade Von Hippel-Lindau disease (vHL)WAGR syndrome Williams syndrome X-linked hypophosphatemic rickets (XLHR)Xanthinuria type I Xanthinuria type II

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