| children | - Acrorenal mandibular syndrome 720414005
- Acrorenal syndrome 720458005
- Acrorenoocular syndrome 720415006
- Aniridia, renal agenesis, psychomotor retardation syndrome 733116005
- Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome 720519003
- Autosomal dominant intermediate Charcot-Marie-Tooth disease type E 722294004
- Autosomal dominant polycystic kidney disease 765330003
- Autosomal dominant progressive nephropathy with hypertension 703310005
- Autosomal dominant tubulointerstitial kidney disease 726018006
- Bartter syndrome 707742001
- Cerebral ventriculomegaly, cystic kidney disease 1216942009
- Congenital nephrotic syndrome 48796009
- Congenital nephrotic syndrome due to congenital infection 722118005
- Congenital nephrotic syndrome due to diffuse mesangial sclerosis 722369003
- Congenital nephrotic syndrome with focal glomerulosclerosis 236384008
- Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome 733453005
- Congenital neutropenia, myelofibrosis, nephromegaly syndrome 775909002
- Congenital vertebral, cardiac, renal anomalies syndrome 1260142000
- Crome syndrome 722381004
- Cystinuria, type 1 37183000
- Dent's disease 444645005
- Diffuse mesangial sclerosis with ocular abnormalities 236528009
- Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis 783620009
- Drash syndrome 236385009
- Dysmorphic sialidosis with renal involvement 81896006
- Enamel-renal syndrome 109477002
- Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome 763280005
- Fabry's disease 16652001
- Faciocardiorenal syndrome 723333000
- Familial amyloid nephropathy with urticaria AND deafness 15123008
- Familial arthrogryposis-cholestatic hepatorenal syndrome 62216007
- Familial hypokalemic alkalosis, Gullner type 81987005
- Familial papillary thyroid carcinoma with renal papillary neoplasia syndrome 716657000
- Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement 725033008
- Familial renal cell carcinoma 717736007
- Familial renal iminoglycinuria 75652008
- Familial steroid-resistant nephrotic syndrome with adrenal insufficiency 1187040004
- Familial steroid-resistant nephrotic syndrome with sensorineural deafness 783614008
- Fibronectin glomerulopathy 818952002
- Galloway Mowat syndrome 721297008
- Genetic steroid-resistant nephrotic syndrome 718141008
- Gitelman syndrome 707756004
- Glycogenosis with glucoaminophosphaturia 61598006
- HELIX syndrome 1217380005
- Hereditary diffuse crescentic glomerulonephritis 367521000119108
- Hereditary focal and segmental glomerular lesions 367571000119109
- Hereditary minor glomerular abnormality 367581000119107
- Hereditary nephritis 399340005
- Hereditary nephrogenic diabetes insipidus 61165007
- Hereditary tubulointerstitial disorder 78815005
- Hereditary xanthinuria 54627004
- Holzgreve syndrome 783159001
- Hyperuricemia, anemia, renal failure syndrome 721840000
- Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome 776416004
- Hypoparathyroidism, deafness, renal disease syndrome 724282009
- Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome 723363009
- Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome 733097003
- Infantile nephropathic cystinosis 62332007
- Infundibulopelvic stenosis multicystic kidney syndrome 725905005
- Inherited magnesium-losing nephropathy 236480003
- Inherited renal tubule insufficiency with cholestatic jaundice 236482006
- Joubert syndrome with renal defect 716999001
- Juvenile cataract, microcornea, renal glucosuria syndrome 722457005
- Karyomegalic interstitial nephritis 782738008
- LAMB2-related infantile-onset nephrotic syndrome 771447009
- Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome 1237470001
- Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome 1237342004
- Lipoprotein glomerulopathy 446923008
- Lowe syndrome 79385002
- MARCH syndrome 1169358003
- Melnick-Fraser syndrome 290006
- Mitochondrial DNA depletion syndrome hepatocerebrorenal form 782771007
- Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome 724094005
- Nephrogenic syndrome of inappropriate antidiuresis 723440000
- Nephronophthisis 204958008
- Nephropathy, deafness, hyperparathyroidism syndrome 724093004
- Neurofaciodigitorenal syndrome 725908007
- Non-progressive hereditary glomerulonephritis 399190000
- NPHP3-related Meckel-like syndrome 773737004
- Oligohydramnios sequence 41962002
- Perlman syndrome 722231005
- Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome 721970009
- Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction 237612000
- Pierson syndrome 723449004
- Polycystic kidney disease, infantile type 28770003
- Primary hyperoxaluria 17901006
- Proximal tubulopathy, diabetes mellitus, cerebellar ataxia syndrome 724062000 removed: 2020-01-31
- Radio-renal syndrome 766765009
- Renal carnitine transport defect 21764004
- Renal coloboma syndrome 446449009
- Renal hepatic pancreatic dysplasia 763891005
- Renal phosphaturia 85487008
- Renal tubular acidosis with progressive nerve deafness 236532003
- Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations 783787000
- RHYNS syndrome 723999009
- Saito Kuba Tsuruta syndrome 716094008
- Saldino-Mainzer dysplasia 254092004
- Schimke immuno-osseous dysplasia 723995003
- Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome 721207002
- SERKAL syndrome 723720008
- Severe oculo-renal-cerebellar syndrome 1208341008
- Spastic paraplegia, nephritis, deafness syndrome 733089005
- Thin basement membrane disease 236418003
- Thymic, renal, anal, lung dysplasia syndrome 723555007
- Thyrocerebrorenal syndrome 733096007
- Torticollis, keloids, cryptorchidism, renal dysplasia syndrome 771266007
- Tubular renal disease with cardiomyopathy syndrome 719839000
- Ulbright Hodes syndrome 719840003
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