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| Term | nephronophthisis | ID (Ontology) | DOID:12712 (Human Disease) |
| Definition | A kidney disease that is characterized by a chronic tubulointerstitial nephritis that progress to terminal renal failure during the second decade (juvenile form) or before the age of 5 years (infantile form) resulting from dysfunction of ciliary proteins (ciliopathy). | ||
| Also Known As | "medullary cystic disease" ; "medullary cystic kidney" | ||
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autosomal genetic disease |__autosomal recessive disease__ urinary system disease | |__kidney disease_______________| nephronophthisis 10 rec. |__nephronophthisis 1 |__nephronophthisis 2 |__nephronophthisis 3 |__nephronophthisis 4 |__nephronophthisis 7 1 rec. |__nephronophthisis 9 1 rec. |__nephronophthisis 11 1 rec. |__nephronophthisis 12 |__nephronophthisis 13 1 rec. |__nephronophthisis 14 1 rec. |__nephronophthisis 15 1 rec. |__nephronophthisis 16 1 rec. |__nephronophthisis 18 |__nephronophthisis 19 |__nephronophthisis 20 1 rec. |__nephronophthisis-like nephropathy 1 2 rec. |
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| Is a |
autosomal recessive disease kidney disease |
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GARD:206 ICD10CM:Q61.5 MIM:PS256100 NCI:C123200 ORDO:655 SNOMEDCT_US_2023_03_01:204958008 UMLS_CUI:C0687120 |
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