fibronectin glomerulopathy
Fibronectin glomerulopathy is a hereditary kidney disease characterized by proteinuria, type IV renal tubular acidosis, microscopic hematuria and hypertension that may lead to end-stage renal failure in the second to sixth decade of life
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fibronectin glomerulopathy
Summary
fibronectin glomerulopathy is a rare disease[1].
Key Facts
- fibronectin glomerulopathy's instance of is recorded as rare disease[2].
- fibronectin glomerulopathy's instance of is recorded as class of disease[3].
- fibronectin glomerulopathy's subclass of is recorded as glomerulopathy[4].
- fibronectin glomerulopathy's MeSH descriptor ID is recorded as C536826[5].
- fibronectin glomerulopathy's MeSH descriptor ID is recorded as C562900[6].
- fibronectin glomerulopathy's KEGG ID is recorded as H01260[7].
- fibronectin glomerulopathy's Orphanet ID is recorded as 84090[8].
- fibronectin glomerulopathy's genetic association is recorded as FN1[9].
- fibronectin glomerulopathy's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_84090[10].
- fibronectin glomerulopathy's UMLS CUI is recorded as C3888104[11].
- fibronectin glomerulopathy's UMLS CUI is recorded as C1866075[12].
- fibronectin glomerulopathy's ICD-10-CM is recorded as N07.6[13].
- fibronectin glomerulopathy's PatientsLikeMe condition ID is recorded as fibronectin-glomerulopathy[14].
- fibronectin glomerulopathy's GARD rare disease ID is recorded as 9268[15].
- fibronectin glomerulopathy's Mondo ID is recorded as MONDO_0007671[16].
- fibronectin glomerulopathy's ICD-11 ID is recorded as MF81[17].
- fibronectin glomerulopathy's Genetics Home Reference Conditions ID is recorded as fibronectin-glomerulopathy[18].
- fibronectin glomerulopathy's ICD-11 ID is recorded as 1877494378[19].