Hereditary disorder of the urinary system
Kidney disease
||
Hereditary nephropathy (disorder)
Hereditary nephropathy
Hereditary disorder of kidney
Inherited renal disease
Id367591000119105
StatusDefined
Finding siteKidney structure
RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set
TargetN07.9
TermHereditaire nefropathie, niet elders geclassificeerd; niet gespecificeerd
SNOMED CT to ICD-10 extended map
TargetN07.9
RuleTRUE
AdviceALWAYS N07.9 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
|
Acrorenal mandibular syndrome
Acrorenal syndrome
Acrorenoocular syndrome
Aniridia, renal agenesis, psychomotor retardation syndrome
Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
Autosomal dominant polycystic kidney disease5
Autosomal dominant progressive nephropathy with hypertension
Autosomal dominant tubulointerstitial kidney disease2
Bartter syndrome4
Cerebral ventriculomegaly, cystic kidney disease
Congenital nephrotic syndrome2
Congenital nephrotic syndrome due to congenital infection
Congenital nephrotic syndrome due to diffuse mesangial sclerosis
Congenital nephrotic syndrome with focal glomerulosclerosis
Congenital nephrotic syndrome, interstitial lung disease, epidermolysis bullosa syndrome
Congenital neutropenia, myelofibrosis, nephromegaly syndrome
Congenital vertebral, cardiac, renal anomalies syndrome
Crome syndrome
Cystinuria, type 13
Dent's disease3
Dibasic amino aciduria type 1
Diffuse mesangial sclerosis with ocular abnormalities
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis
Drash syndrome
Dysmorphic sialidosis with renal involvement
EGF-related primary hypomagnesemia with intellectual disability
Enamel-renal syndrome
Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome
Fabry's disease
Faciocardiorenal syndrome
Familial amyloid nephropathy with urticaria AND deafness
Familial arthrogryposis-cholestatic hepatorenal syndrome
Familial hypokalemic alkalosis, Gullner type
Familial juvenile hyperuricemic nephropathy
Familial papillary thyroid carcinoma with renal papillary neoplasia syndrome
Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis2
Familial renal cell carcinoma1
Familial renal iminoglycinuria
Familial steroid-resistant nephrotic syndrome with adrenal insufficiency
Familial steroid-resistant nephrotic syndrome with sensorineural deafness
Fibronectin glomerulopathy2
Galloway Mowat syndrome
Genetic steroid-resistant nephrotic syndrome
Gitelman syndrome
Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation
Glycogenosis with glucoaminophosphaturia
HELIX syndrome
Hepatic fibrosis, renal cyst, intellectual disability syndrome
Hereditary diffuse crescentic glomerulonephritis
Hereditary focal and segmental glomerular lesions
Hereditary minor glomerular abnormality
Hereditary nephritis11
Hereditary podocytopathy
Hereditary tubulointerstitial disorder
Hereditary xanthinuria2
Holzgreve syndrome
Hyperuricemia, anemia, renal failure syndrome
Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome
Hypoparathyroidism, deafness, renal disease syndrome
Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome
Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome
Infantile nephropathic cystinosis1
Infundibulopelvic stenosis multicystic kidney syndrome
Inherited magnesium-losing nephropathy
Inherited renal tubule insufficiency with cholestatic jaundice
Joubert syndrome with renal defect
Juvenile cataract, microcornea, renal glucosuria syndrome
Karyomegalic interstitial nephritis
LAMB2-related infantile-onset nephrotic syndrome
Lethal fetal brain malformation, duodenal atresia, bilateral renal hypoplasia syndrome
Lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome
Lipoprotein glomerulopathy
Lowe syndrome
Lysinuric protein intolerance
MARCH syndrome
Melnick-Fraser syndrome
Mitochondrial DNA depletion syndrome hepatocerebrorenal form
Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome
Nephrogenic syndrome of inappropriate antidiuresis
Nephronophthisis9
Nephropathy, deafness, hyperparathyroidism syndrome
Neurofaciodigitorenal syndrome
Non-progressive hereditary glomerulonephritis
NPHP3-related Meckel-like syndrome
Oligohydramnios sequence
Perlman syndrome
Persistent Mullerian derivative with lymphangiectasia and polydactyly syndrome
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction
Pierson syndrome
Polycystic kidney disease, infantile type
Primary hyperoxaluria3
Radio-renal syndrome
Renal carnitine transport defect
Renal coloboma syndrome
Renal hepatic pancreatic dysplasia
Renal phosphaturia
Renal tubular acidosis with progressive nerve deafness
Renal tubulopathy with encephalopathy and liver failure syndrome
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
RHYNS syndrome
Saito Kuba Tsuruta syndrome
Saldino-Mainzer dysplasia
Schimke immuno-osseous dysplasia
Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome
SERKAL syndrome
Severe oculo-renal-cerebellar syndrome
Spastic paraplegia, nephritis, deafness syndrome
Thymic, renal, anal, lung dysplasia syndrome
Thyrocerebrorenal syndrome
Torticollis, keloids, cryptorchidism, renal dysplasia syndrome
Tubular renal disease with cardiomyopathy syndrome
Ulbright Hodes syndrome