Tooth ankylosis

disease
On this page

Also known as abnormal fusion of dental cementum with alveolar boneankylosis (disease) of calcareous toothankylosis of teethankylosis of toothcalcareous tooth ankylosis (disease)molar I reinclusionsecondary retention of permanent molars

Summary

Tooth ankylosis (MONDO:0008007) is a disease and 1 clinical trial. A subtype of tooth hard tissue disease — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Prevalence: Unknown (Worldwide)
  • Phenotypes (HPO): 4
  • Clinical trials: 1

Clinical features

Signs & symptoms

Clinical features (HPO)

4 HPO clinical features (Orphanet curated; top 4 by frequency):

HPO IDTermFrequency
HP:0009804Tooth agenesisVery frequent (80-99%)
HP:0000682Abnormality of dental enamelFrequent (30-79%)
HP:0000303Mandibular prognathiaOccasional (5-29%)
HP:0004209Clinodactyly of the 5th fingerOccasional (5-29%)

Identifiers

Disease identifiers

FieldValue
Canonical nametooth ankylosis
Mondo IDMONDO:0008007
MeSHD020254
OMIM157950
Orphanet1077
DOIDDOID:12661
ICD-10-CMK03.5
ICD-112066427602
SNOMED CT14901003
UMLSC0155930
MedGen57843
GARD0000701
MedDRA10044019
Anatomy (UBERON)UBERON:0001091
Is cancer (heuristic)no

Also known as: abnormal fusion of dental cementum with alveolar bone · ankylosis (disease) of calcareous tooth · ankylosis of teeth · ankylosis of tooth · calcareous tooth ankylosis (disease) · molar I reinclusion · secondary retention of permanent molars

Disease family

This is a subtype of tooth hard tissue disease. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by body system or component › musculoskeletal system disorderskeletal system disordertooth disordertooth hard tissue diseasetooth ankylosis

Related subtypes (6): tooth resorption, dental enamel hypoplasia, dentin sensitivity, dental caries, hypercementosis, dentin dysplasia

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 1.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07185711Not specifiedCOMPLETEDRFA and Bite Force in COD Teeth

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.