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Regional odontodysplasia

disorder
SNOMED 66063001CUI C0206554

Overview

Regional odontodysplasia is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Research Evidence

Peer-reviewed studies linked via MeSH term "Odontodysplasia" from the MEDLINE/PubMed database.

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Segmental Odontomaxillary Dysplasia: Systematic Review.
[object Object], [object Object], [object Object] et al. · Head Neck Pathol · 2024
PMID: 39436514Meta-AnalysisFull text (PMC)
[Research progress in regional odontodysplasia].
[object Object], [object Object], [object Object] et al. · Zhonghua Kou Qiang Yi Xue Za Zhi · 2024
PMID: 38637007Review
Regional odontodysplasia with facial cellulitis: a case report and literature review.
[object Object], [object Object], [object Object] · Hua Xi Kou Qiang Yi Xue Za Zhi · 2024
PMID: 38475960ReviewFull text (PMC)
Hereditary dentin defects with systemic diseases.
[object Object], [object Object], [object Object] et al. · Oral Dis · 2023
PMID: 37094075Review
Hereditary Disorders of Cardiovascular Calcification.
[object Object], [object Object], [object Object] · Arterioscler Thromb Vasc Biol · 2021
PMID: 33176451Review
RNA Editing in Interferonopathies.
[object Object], [object Object], [object Object] et al. · Methods Mol Biol · 2021
PMID: 32729086Review
Toward a better understanding of type I interferonopathies: a brief summary, update and beyond.
[object Object], [object Object] · World J Pediatr · 2020
PMID: 31377974Review
JAK-inhibitors. New players in the field of immune-mediated diseases, beyond rheumatoid arthritis.
[object Object], [object Object], [object Object] · Rheumatology (Oxford) · 2019
PMID: 30806709ReviewFull text (PMC)
Inherited Arterial Calcification Syndromes: Etiologies and Treatment Concepts.
[object Object], [object Object] · Curr Osteoporos Rep · 2017
PMID: 28585220Review
Type I interferonopathies in pediatric rheumatology.
[object Object], [object Object], [object Object] et al. · Pediatr Rheumatol Online J · 2016
PMID: 27260006ReviewFull text (PMC)

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Abnormal dental pulp morphology
Frequent (30-79%)HP:0006479
Abnormal tooth enamel
Frequent (30-79%)HP:0000682
Abnormality of dental color
Frequent (30-79%)HP:0011073
Abnormality of milk teeth
Frequent (30-79%)HP:0006481
Decreased enamel calcification
Frequent (30-79%)HP:0011084
Delayed eruption of teeth
Frequent (30-79%)HP:0000684
Dental cavities
Frequent (30-79%)HP:0000670
Dentin anomaly
Frequent (30-79%)HP:0010299
Enamel, underdeveloped
Frequent (30-79%)HP:0006297
Eruption failure
Frequent (30-79%)HP:0000706
Jaw pain
Frequent (30-79%)HP:0040264
Pitting of tooth enamel
Frequent (30-79%)HP:0009722
Pulpoliths
Frequent (30-79%)HP:0003771
Red and swollen gums
Frequent (30-79%)HP:0000230
Teeth with type iii dentinogenesis imperfecta
Frequent (30-79%)HP:0000694
Tooth abscess
Frequent (30-79%)HP:0030757
Yellow-brown discolored teeth
Frequent (30-79%)HP:0006286
Failure of eruption of multiple teeth
Occasional (5-29%)HP:0006283
Hyperplasia of alveolar process of jaw
Occasional (5-29%)HP:0009085
Hypertrophy of tooth
Occasional (5-29%)HP:0001572
Hypoplastic teeth
Occasional (5-29%)HP:0000685
Lower jaw pain
Occasional (5-29%)HP:0200025
Oral soft tissue hyperplasia
Occasional (5-29%)HP:0000212
Underdeveloped dental roots
Occasional (5-29%)HP:0006336

Quick Facts

SNOMED CT
66063001
UMLS CUI
C0206554
Fully Specified Name
Regional odontodysplasia (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
24
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.