Overview
Hereditary disease is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Related Conditions
Autosomal hereditary disorder(child)
Polygenic hereditary disorder(child)
Sex-linked hereditary disorder(child)
Developmental hereditary disorder(child)
Hereditary disorder by system(child)
Mendelian disorders(child)
Hereditary hypoplasminogenemia(child)
Hereditary dysplasminogenemia(child)
Hereditary coagulation factor deficiency(child)
Familial hemorrhagic diathesis(child)
Fetus with hereditary disease(child)
Hereditary neoplastic syndrome(child)
Connective tissue hereditary disorder(child)
Obesity due to melanocortin 4 receptor deficiency(child)
Familial thyroglossal duct cyst(child)
Severe congenital hypochromic anemia with ringed sideroblasts(child)
Hereditary amyloidosis(child)
Hereditary vitamin B12 deficiency anemia(child)
Hereditary folate deficiency anemia(child)
Chronic granulomatous disease(child)
Quick Facts
- SNOMED CT
- 32895009
- UMLS CUI
- C0019247
- Fully Specified Name
- Hereditary disease (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.