Familial idiopathic steroid-resistant nephrotic syndrome

disorder

SNOMED 718141008CUI C4273714

Overview

Familial idiopathic steroid-resistant nephrotic syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Proteinuria

Always present (100%)HP:0000093

Edema

Very frequent (80-99%)HP:0000969

CKD

Frequent (30-79%)HP:0012622

End-stage renal disease

Frequent (30-79%)HP:0003774

Focal and segmental glomerulosclerosis

Frequent (30-79%)HP:0000097

Periorbital edema

Frequent (30-79%)HP:0100539

Diffuse mesangial sclerosis glomerulopathy

Occasional (5-29%)HP:0001967

Frothy urine

Occasional (5-29%)HP:0031504

Gastro pain

Occasional (5-29%)HP:0002027

Headache

Occasional (5-29%)HP:0002315

Hypoalbuminaemia

Occasional (5-29%)HP:0003073

Irritable mood

Occasional (5-29%)HP:0000737

Minimal change disease

Occasional (5-29%)HP:0012579

Pyrexia

Occasional (5-29%)HP:0001945

Respiratory infection

Occasional (5-29%)HP:0011947

Abnormality of the nervous system

Very rare (1-4%)HP:0000707

Peritonitis

Very rare (1-4%)HP:0002586

Related Conditions

Steroid-unresponsive nephrotic syndrome(parent)

Hereditary nephropathy(parent)

Genetic disease of glomerulus(parent)

Quick Facts

SNOMED CT: 718141008
UMLS CUI: C4273714
Fully Specified Name: Genetic steroid-resistant nephrotic syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 17

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.