Overview
Rutherfurd 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.
Corneal dystrophy
Very frequent (80-99%)HP:0001131
Delayed eruption of teeth
Very frequent (80-99%)HP:0000684
Gingival hyperplasia
Very frequent (80-99%)HP:0000212
Idiopathic gingival hyperplasia
Very frequent (80-99%)HP:0000169
Chewing difficulties
Frequent (30-79%)HP:0005216
Impaired vision
Frequent (30-79%)HP:0000505
Misshapened teeth
Frequent (30-79%)HP:0006482
Scarring or clouding of the cornea of the eye
Frequent (30-79%)HP:0007957
Cloudy cornea
HP:0007759
Delayed primary teeth eruption
HP:0000680
Failure of eruption of permanent teeth
HP:0006352
Related Conditions
Quick Facts
- SNOMED CT
- 699754008
- UMLS CUI
- C0796140
- Fully Specified Name
- Oculodental syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 11
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.