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236381000: Steroid-resistant nephrotic syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
354334010 Steroid-unresponsive nephrotic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
354335011 SRNS - Steroid-resistant nephrotic syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
354336012 Steroid-resistant nephrotic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
624966015 Steroid-resistant nephrotic syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5010681000241117 syndrome néphrotique résistant aux stéroïdes fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

9 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Steroid-resistant nephrotic syndrome Is a Nephrotic syndrome true Inferred relationship Some
Steroid-resistant nephrotic syndrome Finding site Glomerulus structure true Inferred relationship Some 3
Steroid-resistant nephrotic syndrome Finding site Kidney structure false Inferred relationship Some
Steroid-resistant nephrotic syndrome Has interpretation Above reference range true Inferred relationship Some 1
Steroid-resistant nephrotic syndrome Has interpretation Below reference range true Inferred relationship Some 2
Steroid-resistant nephrotic syndrome Interprets Albumin measurement (procedure) true Inferred relationship Some 2
Steroid-resistant nephrotic syndrome Interprets Measurement of protein in urine (procedure) true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Steroid resistant nephrotic syndrome of childhood Is a True Steroid-resistant nephrotic syndrome Inferred relationship Some
A rare, hereditary nephrotic syndrome characterized by proteinuria, hypoalbuminemia, edema, and hyperlipidemia, with an absence of response to an initial trial of corticosteroids (i.e. steroid-resistant nephrotic syndrome; SRNS) and a generally complicated course. Is a True Steroid-resistant nephrotic syndrome Inferred relationship Some
A rare, genetic multisystem disorder characterized by a neurodegenerative disorder associating global developmental delay, progressive microcephaly, and progressive cerebral and cerebellar atrophy with extrapyramidal involvement, progressive optic atrophy, and in many patients early-onset steroid-resistant nephrotic syndrome. Is a True Steroid-resistant nephrotic syndrome Inferred relationship Some
A rare primary glomerular disease characterized by the association of congenital nephrotic syndrome, early onset renal failure and ocular anomalies with microcoria and severe neurodevelopment deficits. Is a True Steroid-resistant nephrotic syndrome Inferred relationship Some
LAMB2-related infantile-onset nephrotic syndrome Is a True Steroid-resistant nephrotic syndrome Inferred relationship Some
A rare, genetic coenzyme Q10 deficiency characterized by sensorineural deafness and severe, progressive nephrotic syndrome not responding to steroid treatment. Clinical manifestations include early onset proteinuria, hypoalbuminemia and edema, leading to end-stage renal disease. The renal biopsy reveals focal segmental glomerulosclerosis and diffuse mesangial sclerosis. Rarely, seizures, ataxia and dysmorphic features have been described. Is a True Steroid-resistant nephrotic syndrome Inferred relationship Some
A rare disorder with multisystemic involvement and glomerulopathy characterized by progressive steroid-resistant nephrotic syndrome typically associated with focal segmental glomerulosclerosis, as well as primary adrenal insufficiency with adrenal calcifications. Age of onset and disease course are variable, with some cases presenting as severe fetal hydrops, while most patients present in infancy or early childhood and progress to end-stage renal disease within a few years. Additional features include ichthyosis, primary hypothyroidism, hypogonadism, immunodeficiency, and neurological manifestations (such as cognitive impairment, ataxia, sensorineural hearing loss, or seizures). Is a True Steroid-resistant nephrotic syndrome Inferred relationship Some
A rare, idiopathic nephrotic syndrome characterized by the triad of proteinuria, hypoalbuminemia and edema in patients who do not respond, or only partially respond, to the initial trial of corticosteroids. Patients may be multidrug resistant or may be sensitive to second-line immunosuppressive therapy. Is a True Steroid-resistant nephrotic syndrome Inferred relationship Some

This concept is not in any reference sets

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