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Multinodular goiter, cystic kidney, polydactyly syndrome
disorderSNOMED 723409007CUI C1841853
Overview
Multinodular goiter, cystic kidney, polydactyly 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.
Multicystic kidney dysplasia
Frequent (30-79%)HP:0000003
Multinodular goiter
Frequent (30-79%)HP:0005987
Postaxial hand polydactyly
Frequent (30-79%)HP:0001162
Preaxial polydactyly of foot
Frequent (30-79%)HP:0001841
Triphalangy of thumb
Frequent (30-79%)HP:0001199
Related Conditions
Multiple malformation syndrome with limb defect as major feature(parent)
Multinodular goitre(parent)
Hereditary disorder of endocrine system(parent)
Congenital anomaly of digit(parent)
Congenital anomaly of the thyroid gland(parent)
Congenital anomaly of the kidney(parent)
Autosomal dominant polycystic kidney disease(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 723409007
- UMLS CUI
- C1841853
- Fully Specified Name
- Multinodular goiter, cystic kidney, polydactyly syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 5
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.