Hereditary disorder of the urinary system	Kidney disease
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Hereditary nephropathy (disorder)
	Hereditary nephropathy
	Hereditary disorder of kidney Inherited renal disease
	hereditaire nefropathie

Id	367591000119105
Status	Defined

Finding site

Kidney structure

DHD Diagnosis thesaurus reference set

ICD-10 complex map reference set

Target	N07.9
Rule	TRUE
Advice	ALWAYS N07.9 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED 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 nephroblastoma

Congenital nephrotic syndrome3

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

Crome syndrome

Cystinuria, type 12

Dent's disease3

Diffuse mesangial sclerosis with ocular abnormalities

Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis

Drash syndrome

Dysmorphic sialidosis with renal involvement

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 papillary thyroid carcinoma with renal papillary neoplasia syndrome

Familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement

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

Glycogenosis with glucoaminophosphaturia

HELIX syndrome

Hereditary diffuse crescentic glomerulonephritis

Hereditary focal and segmental glomerular lesions

Hereditary minor glomerular abnormality

Hereditary nephritis12

Hereditary nephrogenic diabetes insipidus

Hereditary tubulointerstitial disorder

Holzgreve syndrome

Hyperuricemia, anemia, renal failure syndrome

Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome

Hypoparathyroidism, deafness, renal disease syndrome

Hypoparathyroidism, sensorineural deafness and renal dysplasia 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

Leigh syndrome with nephrotic syndrome

Lipoprotein glomerulopathy

Lowe syndrome

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

Nephropathic cystinosis

Nephropathy, deafness, hyperparathyroidism syndrome

Neurofaciodigitorenal syndrome

Non-progressive hereditary glomerulonephritis

NPHP3-related Meckel-like syndrome

Oligohydramnios sequence1

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

Recurrent nephroblastoma

Renal carnitine transport defect

Renal coloboma syndrome

Renal hepatic pancreatic dysplasia

Renal phosphaturia

Renal tubular acidosis with progressive nerve deafness

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

Thin basement membrane disease

Thymic, renal, anal, lung dysplasia syndrome

Thyrocerebrorenal syndrome

Torticollis, keloids, cryptorchidism, renal dysplasia syndrome

Tubular renal disease with cardiomyopathy syndrome

Ulbright Hodes syndrome