Overview
Oligodontia 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.
Missing more than six teeth
Always present (100%)HP:0000677
Chewing difficulties
Very frequent (80-99%)HP:0005216
Absence of first permanent molar
Frequent (30-79%)HP:0011056
Absence of upper lateral incisor
Frequent (30-79%)HP:0000690
Agenesis of bicuspid
Frequent (30-79%)HP:0011051
Agenesis of central incisor
Frequent (30-79%)HP:0006289
Angle class 2 malocclusion
Frequent (30-79%)HP:0000689
Delayed eruption of permanent teeth
Frequent (30-79%)HP:0000696
Delayed eruption of teeth
Frequent (30-79%)HP:0000684
Small teeth
Frequent (30-79%)HP:0000691
Underdeveloped dental roots
Frequent (30-79%)HP:0006336
Wide-spaced teeth
Frequent (30-79%)HP:0000687
Abnormality of canine
Occasional (5-29%)HP:0011078
Abnormality of deciduous molar morphology
Occasional (5-29%)HP:0006344
Agenesis of mandibular premolar
Occasional (5-29%)HP:0011053
Cleft lip, cleft palate
Occasional (5-29%)HP:0000202
Decreased size of teeth
Occasional (5-29%)HP:0000685
Eclabium
Occasional (5-29%)HP:0012472
Misshapened teeth
Occasional (5-29%)HP:0006482
Peg-shaped maxillary lateral incisors
Occasional (5-29%)HP:0006342
Taurodont
Occasional (5-29%)HP:0000679
Thin dental enamel
Occasional (5-29%)HP:0006297
Vertical facial insufficiency
Occasional (5-29%)HP:0011219
Related Conditions
X-linked oligodontia(child)
Spondyloepimetaphyseal dysplasia, abnormal dentition syndrome(child)
Cleft palate with stapes fixation and oligodontia syndrome(child)
Deafness and oligodontia syndrome(child)
Partial congenital absence of teeth(parent)
Congenital absence of jaw(parent)
Congenital absence of mouth(parent)
Teeth malformation(parent)
Quick Facts
- SNOMED CT
- 787414001
- UMLS CUI
- C4082304
- Fully Specified Name
- Oligodontia (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 23
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.