Overview
Hereditary amyloidosis is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Familial amyloid nephropathy with urticaria AND deafness(child)
Hereditary oculoleptomeningeal amyloid angiopathy(child)
Autosomal dominant beta2-microglobulinic amyloidosis(child)
Chronic diarrhoea with hereditary sensory and autonomic neuropathy(child)
Hereditary gelsolin amyloidosis(child)
Heredofamilial systemic amyloidosis affecting skin(child)
Familial amyloid polyneuropathy(child)
Gelatinous droplike corneal dystrophy(child)
Organ limited hereditary amyloidosis(child)
Hereditary cerebrovascular amyloidosis(child)
ITM2B-related cerebral amyloid angiopathy(child)
Familial transthyretin-related amyloidosis(child)
Hereditary systemic amyloidosis(child)
Amyloidosis(parent)
Hereditary disease(parent)
Quick Facts
- SNOMED CT
- 367601000119103
- UMLS CUI
- C0740340
- Fully Specified Name
- Hereditary amyloidosis (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.