Overview
Faciocardiorenal 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.
Broad flat nasal bridge
Very frequent (80-99%)HP:0000431
Cleft of palate
Very frequent (80-99%)HP:0000175
Dull intelligence
Very frequent (80-99%)HP:0001249
Flat philtrum
Very frequent (80-99%)HP:0000319
Horseshoe kidney
Very frequent (80-99%)HP:0000085
Increased distance between eyes
Very frequent (80-99%)HP:0000316
Missing between one and six teeth
Very frequent (80-99%)HP:0000668
Prominent ear
Very frequent (80-99%)HP:0000411
Rhomboid shaped head
Very frequent (80-99%)HP:0001357
Small nasal alae
Very frequent (80-99%)HP:0000430
Endocardial fibroelastosis
Frequent (30-79%)HP:0001706
Narrow mouth
Occasional (5-29%)HP:0000160
Tricuspid valve prolapse
Occasional (5-29%)HP:0001704
Undergrowth
Occasional (5-29%)HP:0001508
Related Conditions
Congenital heart disease(parent)
Horseshoe kidney(parent)
Multiple malformation syndrome with facial defects as major feature(parent)
Recessive hereditary disorder (autosomal)(parent)
Cardiovascular system hereditary disorder(parent)
Hereditary nephropathy(parent)
Developmental hereditary disorder(parent)
Genetic intellectual disability(parent)
Quick Facts
- SNOMED CT
- 723333000
- UMLS CUI
- C0795936
- Fully Specified Name
- Faciocardiorenal syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 14
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.