Diagnoses - Treeview

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Glomerulopathies (93548.0)
Nephrotic syndrome without extrarenal manifestations (567564.0)
Nephrotic syndrome, idiopathic (357502.0)
Idiopathic steroid-sensitive nephrotic syndrome (69061.0)
Idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance (567546.0)
Idiopathic steroid-resistant nephrotic syndrome (567548.0)
Idiopathic multidrug-resistant nephrotic syndrome (567550.0)
Idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunouppressive therapy (567552.0)
Nephrotic syndrome, genetic (564127.0)
Genetic steroid-resistant nephrotic syndrome (SRNS) (656.0)
Congenital nephrotic syndrome, Finnish type (839.0)
Congenital nephrotic syndrome, no genetic cause specified (97556.0)
Glomerulopathy as part of a syndromic disorder (567562.0)
Denys-Drash syndrome (220.0)
Frasier syndrome (347.0)
Galloway-Mowat syndrome (2065.0)
Schimke immuno-osseous dysplasia (1830.0)
Pierson syndrome (2670.0)
Nail-patella syndrome (2614.0)
Leigh syndrome with nephrotic syndrome (255249.0)
Nephrotic syndrome, familial, steroid-resistant (SRNS), with sensorineural deafness (280406.0)
MYH9-related disease (182050.0)
Familial steroid-resistant nephrotic syndrome with adrenal insufficiency (506334.0)
Nephrotic syndrome-deafness-pretibial epidermolysis bullosa syndrome (300333.0)
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome (306504.0)
Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome (69735.0)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (93114.0)
Severe oculo-renal-cerebellar syndrome (2715.0)
Action myoclonus-renal failure syndrome (163696.0)
Fibronectin glomerulopathy (84090.0)
Lipoprotein glomerulopathy (329481.0)
Collagen type III glomerulopathy (84087.0)
Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization (69063.0)
Nephrotic syndrome, syndromic, not otherwise specified (9999972.0)
IgA nephropathy (9999982.0)
Membranous glomerulonephritis (97560.0)
Collagenopathies (inc. Alport syndrome) (544590.0)
Alport syndrome (63.0)
Alport syndrome, X-linked (88917.0)
Alport syndrome, X-linked with diffuse leiomyomatosis (1018.0)
Alport syndrome, autosomal dominant (88918.0)
Alport syndrome, autosomal recessive (88919.0)
Alport syndrome, digenic (9999965.0)
Microscopic (including familial) hematuria (9999976.0)
Collagenopathy, not further specified (9999977.0)
HANAC syndrome (73229.0)
Primary membranoproliferative glomerulonephritis (MPGN) (54370.0)
Immunoglobulin-mediated membranoproliferative glomerulonephritis (MPGN) (329903.0)
C3 glomerulopathy (329918.0)
Dense deposit disease (93571.0)
C3 glomerulonephritis (329931.0)
Immune complex associated membranoproliferative glomerulonephritis (MPGN), not otherwise specified (9999975.0)
Glomerulopathy as part of a systemic disorder (567554.0)
Glomerulopathy as part of a genetic systemic disease (567556.0)
Familial Mediterranean fever (342.0)
Muckle-Wells syndrome (575.0)
Hypocomplementemic urticarial vasculitis (36412.0)
Hereditary amyloidosis with primary renal involement (85450.0)
AApoAI amyloidosis (93560.0)
ALys amyloidosis (93561.0)
AFib amyloidosis (93562.0)
AApoAII amyloidosis (238269.0)
Autoimmune interstitial lung disease-arthritis syndrome (444092.0)
Glomerulopathy as part of a non-genetic systemic disease (567558.0)
Systemic vasculitis associated with glomerulopathy (567560.0)
Systemic Lupus Erythematosus (SLE) (536.0)
Childhood-onset systemic lupus erythematosus (SLE) (93552.0)
Granulomatosis with polyangiitis (Wegener) (900.0)
Immunoglobulin A vasculitis (Henoch Schonlein nephritis, PSH) (761.0)
Pauci-immune glomerulonephritis (93126.0)
Pauci-immune glomerulonephritis with ANCA (97563.0)
Pauci-immune glomerulonephritis without ANCA (97564.0)
Microscopic polyangiitis (727.0)
Eosinophilic granulomatosis with polyangiitis (183.0)
Polyarteritis nodosa (767.0)
Takayasu arteritis (3287.0)
Giant cell arteritis (397.0)
Relapsing polychondritis (728.0)
Buerger disease (36258.0)
Cryoglobulinemic vasculitis (91138.0)
Anti-glomerular basement membrane disease (375.0)
Mixed connective tissue disease (809.0)
Monoclonal gammopathy of renal significance (MGRS) (9999974.0)
C3 glomerulopathy secondary to MGRS (9999970.0)
Proliferative glomerulonephritis with monoclonal immune deposits (PGNMID) (9999971.0)
AA amyloidosis (85445.0)
AL amyloidosis (85443.0)
Primary systemic amyloidosis (314701.0)
Primary localized amyloidosis (314709.0)
AH amyloidosis (442582.0)
AApoAIV amyloidosis (439232.0)
Non-amyloid monoclonal immunoglobulin deposition disease (86861.0)
Heavy chain deposition disease (93556.0)
Light and heavy chain deposition disease (93557.0)
Light chain deposition disease (93558.0)
IgG4-related kidney disease (449395.0)
Polymyositis (732.0)
Juvenile polymyositis (93568.0)
Dermatomyositis (221.0)
Juvenile dermatomyositis (93672.0)
Beh (117.0)
Sarcoidosis (797.0)
Adult-onset Still disease (829.0)
Reynolds syndrome (779.0)
Systemic sclerosis (90291.0)
CREST syndrome (90290.0)
Diffuse cutaneous systemic sclerosis (220393.0)
Limited cutaneous systemic sclerosis (220402.0)
Limited systemic sclerosis (220407.0)
Immunotactoid or fibrillary glomerulopathy (91137.0)
Non-amyloid fibrillary glomerulopathy (97566.0)
Immunotactoid glomerulopathy (97567.0)
Idiopathic non-lupus full-house nephropathy (567544.0)
Tubulopathies (93603.0)
Primary renal tubular acidosis (314822.0)
Proximal renal tubular acidosis (47159.0)
Autosomal dominant proximal renal tubular acidosis (314889.0)
Autosomal recessive proximal renal tubular acidosis (93607.0)
Osteopetrosis with renal tubular acidosis (2785.0)
Distal renal tubular acidosis (18.0)
Autosomal dominant distal renal tubular acidosis (dRTA) (93608.0)
Autosomal recessive distal renal tubular acidosis (dRTA) (402041.0)
Distal renal tubular acidosis with hemolytic anemia (93610.0)
Auto-immune distal renal tubular acidosis (9999994.0)
Sjogren Syndrome (289390.0)
Primary biliary cholangitis (186.0)
Autoimmune hepatitis (2137.0)
Other autoimmune dRTA (9999966.0)
Cystinuria (214.0)
Hypotonia-cystinuria syndrome (163690.0)
Bartter syndrome (112.0)
Bartter syndrome, transient (570371.0)
Hypokalemic alkalosis, CLDN10 associated (528105.0)
Gitelman syndrome (358.0)
Genetic primary hypomagnesemia (34526.0)
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis (306516.0)
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement (2196.0)
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement (31043.0)
Genetic primary hypomagnesemia with normocalcuria (306522.0)
Familial primary hypomagnesemia with normocalciuria and normocalcemia (34527.0)
Isolated autosomal dominant hypomagnesemia, Glaudemans type (199326.0)
Primary hypomagnesemia with secondary hypocalcemia (30924.0)
Familial primary hypomagnesemia with hypocalcuria (306519.0)
Autosomal dominant primary hypomagnesemia with hypocalciuria (34528.0)
Primary hypomagnesemia with refractory seizures and intellectual disability (564178.0)
Hypomagnesaemia, drug-induced (9999992.0)
Fanconi syndrome, primary (3337.0)
Fanconi syndrome, drug induced (9999996.0)
Fanconi syndrome, Cisplatin induced (240863.0)
Fanconi syndrome, induced by other drug (9999967.0)
Fanconi syndrome, heavy metal induced (9999998.0)
Fanconi syndrome, lead induced (330015.0)
Fanconi syndrome, mercury induced (330021.0)
Faconi syndrome, induced by other heavy metal (9999997.0)
Fanconi syndrome, monoclonal Ig light chain-associated (91136.0)
Hypophosphatemic rickets (437.0)
X-linked hypophosphatemic rickets (XLHR) (89936.0)
Autosomal recessive hypophosphatemic rickets (289176.0)
Autosomal dominant hypophosphatemic rickets (89937.0)
Hereditary hypophosphatemic rickets with hypercalciuria (157215.0)
Hypophosphatemia, dominant, with nephrolithiasis or osteoporosis (244305.0)
Hypercalciuria, idiopathic (2197.0)
Oncogenic osteomalacia (352540.0)
Nephrogenic diabetes insipidus (223.0)
Nephrogenic syndrome of inappropriate antidiuresis (93606.0)
Tubulointerstitial nephritis and uveitis syndrome (91500.0)
Familial renal glucosuria (69076.0)
Pseudohypoaldosteronism type 1 (756.0)
Generalized pseudohypoaldosteronism type 1 (171876.0)
Renal pseudohypoaldosteronism type 1 (171871.0)
EAST syndrome (199343.0)
Arthrogryposis-renal dysfunction-cholestasis (ARC) syndrome (2697.0)
Autosomal dominant hypocalcemia (428.0)
Hereditary renal hypouricemia (94088.0)
Metabolic nephropathies (93593.0)
Dent disease (1652.0)
Dent disease type 1 (CLCN5-related) (93622.0)
Dent disease type 2 (OCRL-related) (93623.0)
Lowe syndrome (534.0)
Nephropathic cystinosis (213.0)
Infantile nephropathic cystinosis (411629.0)
Juvenile nephropathic cystinosis (411634.0)
Primary hyperoxaluria (416.0)
Primary hyperoxaluria type 1 (PH1) (93598.0)
Primary hyperoxaluria type 2 (PH2) (93599.0)
Primary hyperoxaluria type 3 (PH3) (93600.0)
Autosomal recessive infantile hypercalcemia (300547.0)
Amelogenesis imperfecta-nephrocalcinosis syndrome (1031.0)
Fabry disease (324.0)
Tubulopathy due to mitochondrial oxidative phosphorylation disorder (223713.0)
Methylmalonic acidemia (without homocystinuria) (293355.0)
Methylmalonic acidemia, Vitamin B12-responsive (28.0)
Methylmalonic acidemia, Vitamin B12-unresponsive (27.0)
Glycogen storage disease due to glucose-6-phosphatase deficiency (364.0)
Glycogen storage disease due to GLUT2 deficiency (2088.0)
Lysinuric protein intolerance (470.0)
Hereditary xanthinuria (3467.0)
Xanthinuria type I (93601.0)
Xanthinuria type II (93602.0)
Hypoxanthine-guanine phosphoribosyltransferase deficiency (206428.0)
Phosphoribosylpyrophosphate synthetase superactivity (3222.0)
LCAT deficiency (650.0)
Adenine phosphoribosyltransferase deficiency (976.0)
Galactosemia (352.0)
Thrombotic microangiopathies (93573.0)
Hemolytic uremic syndrome (HUS) (544458.0)
Infection-related hemolytic uremic syndrome (HUS) (544482.0)
Shiga toxin-associated hemolytic uremic syndrome (STEC-HUS) (90038.0)
Streptoccous pneumoniae-associated hemolytic uremic syndrome (HUS) (544493.0)
Atypical hemolytic uremic syndrome (aHUS) (2134.0)
Atypical hemolytic uremic syndrome (aHUS) with anti-factor H antibodies (93581.0)
Atypical hemolytic uremic syndrome (aHUS) with complement gene abnormality (544472.0)
Atypical hemolytic uremic syndrome (aHUS), not further specified (9999987.0)
Atypical hemolytic uremic syndrome (aHUS) due to Methylcobalamin deficiency, type CblC (79282.0)
Atypical hemolytic uremic syndrome (aHUS) with DGKE deficiency (357008.0)
Thrombotic thrombocytopenic purpura (TTP) (54057.0)
Congenital thrombotic thrombocytopenic purpura (TTP) (93583.0)
Acquired thrombotic thrombocytopenic purpura (TTP) (93585.0)
Systemic Lupus Erythematosus associated TMA (SLE) (536.1)
Childhood-onset systemic lupus erythematosus associated TMA (SLE) (93552.1)
De novo thrombotic microangiopathy after kidney transplantation (244275.0)
Renal or urinary tract malformations (93545.0)
Non-syndromic renal or urinary tract malformation (93546.0)
Renal agenesis (411709.0)
Renal agenesis, unilateral (93100.0)
Renal agenesis, bilateral (1848.0)
Renal hypoplasia (93101.0)
Renal hypoplasia, unilateral (97361.0)
Renal hypoplasia, bilateral (97362.0)
Oligomeganephronia (2260.0)
Renal dysplasia (93108.0)
Renal dysplasia, unilateral (93172.0)
Renal dysplasia, bilateral (93173.0)
Multicystic dysplastic kidney (1851.0)
Unilateral multicystic dysplastic kidney (97363.0)
Bilateral multicystic dysplastic kidney (97364.0)
Medullary sponge kidney (1309.0)
Renal tubular dysgenesis (3033.0)
Renal tubular dysgenesis of genetic origin (97369.0)
Drug-related renal tubular dysgenesis (97368.0)
Renal tubular dysgenesis due to twin-twin transfusion (97367.0)
Vesicoureteric reflux (VUR), high-grade (9999969.0)
Vesicoureteric reflux (VUR), familial (289365.0)
Fetal lower urinary tract obstruction (LUTO) (435365.0)
Posterior urethral valve (PUV) (93110.0)
Atresia of urethra (105.0)
Prune belly syndrome (2970.0)
Anterior urethral valve (435372.0)
Congenital hydronephrosis (2190.0)
Congenital primary megaureter (617.0)
Ureteropelvic junction (UPJ) obstruction (bilateral or in solitary kidney) (9999985.0)
Congenital primary megaureter, obstructed form (238646.0)
Congenital primary megaureter, refluxing form (238650.0)
Congenital primary megaureter, refluxing and obstructed (9999986.0)
Congenital primary megaureter, nonrefluxing and unobstructed form (238654.0)
Primary megaureter, adult-onset form (238642.0)
Neurogenic bladder, congenital or acquired (9999968.0)
Megacystis-megaureter syndrome (238637.0)
Exstrophy-epispadias complex (322.0)
Bladder exstrophy (93930.0)
Cloacal exstrophy (93929.0)
Epispadias (93928.0)
Syndromic renal or urinary tract malformation (93547.0)
Acro-pectoro-renal dysplasia (956.0)
Acroosteolysis dominant type (955.0)
Acrorenal syndrome (971.0)
Alagille syndrome (52.0)
Aniridia-renal agenesis-psychomotor retardation syndrome (1064.0)
AREDYLD (acral-renal-ectodermal-dysplasia-lipoatrophic-diabetes) syndrome (1133.0)
Bardet-Biedl syndrome (renal / urinary tract malformation) (110.1)
Beckwith-Wiedemann syndrome (116.0)
BOR (branchio-oto-renal) syndrome (107.0)
Cat-eye syndrome (195.0)
Caudal regression sequence (3027.0)
CHARGE syndrome (138.0)
Cornelia de Lange syndrome (96095.0)
Di George syndrome (22q11.2 deletion) (567.0)
EEC (Ectrodactyly-ectodermal dysplasia-cleft lip/palate) syndrome (1896.0)
Fraser syndrome (2052.0)
HDR (Hypoparathyroidism-deafness-renal disease) syndrome (2237.0)
Holoprosencephaly-radial heart renal anomalies syndrome (3186.0)
Infundibulopelvic stenosis-multicystic kidney syndrome (1849.0)
Jeune syndrome (renal / urinary tract malformation) (474.1)
Kallmann syndrome (478.0)
Mayer-Rokitansky-K (3109.0)
Meckel syndrome (renal / urinary tract malformation) (564.1)
Megacystis-microcolon-intestinal hypoperistalsis syndrome (2241.0)
Multicentric carpo-tarsal osteolysis with or without nephropathy (2774.0)
Noonan syndrome (648.0)
Ochoa syndrome (2704.0)
OFD (Orofaciodigital) syndrome type 1 (2750.0)
Pallister-Hall syndrome (672.0)
RCAD (Renal cysts and diabetes) syndrome (93111.0)
Renal coloboma syndrome (1475.0)
Renal nutcracker syndrome (71273.0)
Rubinstein-Taybi syndrome (783.0)
Schinzel-Giedion syndrome (798.0)
SERKAL syndrome (139466.0)
Simpson-Golabi-Behmel syndrome (373.0)
Smith-Lemli-Opitz syndrome (818.0)
Thyrocerebrorenal syndrome (3327.0)
Townes-Brocks syndrome (857.0)
Trisomy 13 (3378.0)
Trisomy 18 (3380.0)
Turner syndrome (881.0)
VACTERL/VATER association (887.0)
WAGR syndrome (893.0)
BNAR (Bifid nose, anorectal and renal anomalies) syndrome (217266.0)
Kabuki Syndrome (2322.0)
Hereditary cystic renal diseases (ciliopathies) (93587.0)
Autosomal dominant tubulointerstitial kidney disease (ADTKD) (34149.0)
UMOD-related autosomal dominant tubulointerstitial kidney disease (ADTKD) (88950.0)
MUC1-related autosomal dominant tubulointerstitial kidney disease (ADTKD) (88949.0)
REN-related autosomal dominant tubulointerstitial kidney disease (ADTKD, FJHN type 1) (217330.0)
HNF1B-related autosomal dominant tubulointerstitial kidney disease (ADTKD) (93111.2)
Autosomal dominant polycystic kidney disease (ADPKD) (730.0)
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (ADPKD-TSC) (88924.0)
Tuberous sclerosis complex (TSC) (805.0)
Von Hippel-Lindau disease (vHL) (892.0)
Autosomal recessive polycystic kidney disease (ARPKD) (731.0)
Nephronophthisis (655.0)
Infantile nephronophthisis (93591.0)
Juvenile nephronophthisis (93592.0)
Late-onset nephronophthisis (93589.0)
Bardet-Biedl syndrome (110.0)
Jeune syndrome (ciliopathies) (474.0)
Joubert syndrome with oculorenal defect (2318.0)
Joubert syndrome with renal defect (220497.0)
Senior-Loken syndrome (3156.0)
Senior-Boichis syndrome (84081.0)
Saldino-Mainzer (conorenal) syndrome (140969.0)
Meckel syndrome (ciliopathies) (564.0)
Cerebrorenodigital (Meckel-like) syndrome (1396.0)
Cranioectodermal dysplasia (Sensenbrenner syndrome) (1515.0)
Ellis van Creveld syndrome (289.0)
Alstr (64.0)
Renal-hepatic-pancreatic dysplasia (294415.0)
RHYNS (retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysaplasia) syndrome (140976.0)
Neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome (79118.0)
Karyomegalic interstitial nephritis (401996.0)
Lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome (444069.0)
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome (439897.0)
Paediatric Chronic Kidney Disease (10000007.0)
Paediatric Dialysis (10000008.0)
Paediatric Transplantation (10000009.0)
Rare causes of hypertension (93618.0)
Renal artery stenosis, congenital (97598.0)
Genetic hypertension involving tubular dysfunction (156629.0)
Apparent mineralocorticoid excess (320.0)
Familial hyperaldosteronism (235936.0)
Familial hyperaldosteronism type I (glucocorticoid-sensitive hypertension) (403.0)
Familial hyperaldosteronism type II (404.0)
Familial hyperaldosteronism type III (251274.0)
Williams syndrome (904.0)
Neurofibromatosis type 1 (636.0)
Pseudohypoaldosteronism type 2 (757.0)
Liddle Syndrome (526.0)
Brachydactyly-arterial hypertension syndrome (1276.0)


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