Overview
Stoelinga de Koomen Davis 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.
Delayed eruption of teeth
Very frequent (80-99%)HP:0000684
Genu valga
Very frequent (80-99%)HP:0002857
Hypotrophic alveolar process of jaw
Very frequent (80-99%)HP:0006329
Hypotrophic malar bone
Very frequent (80-99%)HP:0000272
Maxillozygomatic hypoplasia
Very frequent (80-99%)HP:0005439
Misshapened teeth
Very frequent (80-99%)HP:0006482
Missing between one and six teeth
Very frequent (80-99%)HP:0000668
Posteriorly angulated ears
Frequent (30-79%)HP:0000358
Related Conditions
Multiple malformation syndrome with facial-limb defects as major feature(parent)
Recessive hereditary disorder (autosomal)(parent)
Congenital genu valgum(parent)
Failure of tooth eruption(parent)
Congenital anomaly of bone and joint(parent)
Congenital abnormality of external ear(parent)
Auditory system hereditary disorder(parent)
Hereditary disorder of musculoskeletal system(parent)
Congenital anomaly of jaw(parent)
Developmental hereditary disorder(parent)
Congenital anomaly of face bones(parent)
Hereditary disorder of tooth(parent)
Disorder of digestive system specific to fetus OR newborn(parent)
Abnormal jaw bone morphology(parent)
Quick Facts
- SNOMED CT
- 723442008
- UMLS CUI
- C2931509
- Fully Specified Name
- Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 8
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.