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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
IgA vasculitis (Henoch Schonlein nephritis, PSH)
IgG4-related kidney disease
Imerslund-Gräsbeck syndrome
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)
Structural heart defects-renal anomalies (SHDRA) syndrome
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