Familial arthrogryposis-cholestatic hepatorenal syndrome

disorder

SNOMED 62216007CUI C0268420

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Hepatorenal syndrome(parent)

Familial disease(parent)

Inherited arthrogryposis(parent)

Digestive system hereditary disorder(parent)

Inherited disorder of bilirubin metabolism(parent)

Hereditary nephropathy(parent)

Metabolic renal disease(parent)

Disorder of digestive system specific to fetus OR newborn(parent)

Quick Facts

SNOMED CT: 62216007
UMLS CUI: C0268420
Fully Specified Name: Familial arthrogryposis-cholestatic hepatorenal syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.