Overview
Schmitt Gillenwater Kelly 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.
Abnormal dermatoglyphics
Very frequent (80-99%)HP:0007477
Hypospadias
Very frequent (80-99%)HP:0000047
Increased size of mandible
Very frequent (80-99%)HP:0000303
Micromelia
Very frequent (80-99%)HP:0002983
Nonopposable triphalangeal thumb
Very frequent (80-99%)HP:0005725
Shortening of radius
Very frequent (80-99%)HP:0002984
Gaps between teeth
HP:0000699
Related Conditions
Autosomal dominant hereditary disorder(parent)
Congenital hypoplasia of radius(parent)
Triphalangeal thumb(parent)
Hereditary disorder of musculoskeletal system(parent)
Hereditary disorder of the urinary system(parent)
Hypospadias(parent)
Developmental hereditary disorder(parent)
Hereditary disorder of tooth(parent)
Disorder of digestive system specific to fetus OR newborn(parent)
Quick Facts
- SNOMED CT
- 716092007
- UMLS CUI
- C1867397
- Fully Specified Name
- Radial hypoplasia and triphalangeal thumb with hypospadias and maxillary diastema syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 7
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.