Fissured tongue

disease
On this page

Also known as congenital fissure of tonguecongenital plicated tongueectopic geographic tongueerythema migransfissure of tongue, congenitalFurrowed tongueplicated tonguescrotal tongue

Summary

Fissured tongue (MONDO:0007655) is a disease and 12 clinical trials. Top therapeutic interventions include doxycycline anhydrous, amoxicillin, and cefuroxime axetil. A subtype of tongue disorder — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 12

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namefissured tongue
Mondo IDMONDO:0007655
MeSHD014063
OMIM137400
DOIDDOID:11514
ICD-10-CMK14.5
ICD-11699700094
SNOMED CT52368004
UMLSC4540616
MedGen1624209
Is cancer (heuristic)no

Also known as: congenital fissure of tongue · congenital plicated tongue · ectopic geographic tongue · erythema migrans · fissure of tongue, congenital · Furrowed tongue · plicated tongue · scrotal tongue

Disease family

This is a subtype of tongue disorder. 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 › mouth disordertongue disorderfissured tongue

Related subtypes (8): hypertrophy of tongue papillae, glossitis, hairy tongue, ankyloglossia, isolated congenital hypoglossia/aglossia, digestive duplication cyst of the tongue, tongue neoplasm, glossodynia

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: 12.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified9
PHASE42
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01368341PHASE4COMPLETEDComparing 3 Antibiotic Regimes for Erythema Migrans in General Practice
NCT01518192PHASE4COMPLETEDComparison of Doxycycline and Cefuroxime Axetil for Treatment of Erythema Migrans: Clinical and Microbiological Outcome
NCT03966014PHASE3RECRUITINGDifferent Amoxicillin Treatment Regimens in Erythema Migrans Patients
NCT03462329Not specifiedRECRUITINGPatient’s Pretreatment Expectations About Post-Lyme Symptoms
NCT00132327Not specifiedCOMPLETEDAnalysis of Lyme Disease Lesions
NCT02145754Not specifiedCOMPLETEDCulture Media for Borrelia Burgdorferi Sensu Lato
NCT02147249Not specifiedUNKNOWNCytokines and Chemokines in Erythema Migrans
NCT02414789Not specifiedCOMPLETEDLyme Borreliosis and Early Cutaneous Diagnostic
NCT03371563Not specifiedCOMPLETEDErythema Migrans in Elderly
NCT03505879Not specifiedCOMPLETEDNext Generation Sequencing Detection of Lyme Disease
NCT03956212Not specifiedCOMPLETEDInflammatory Mediators in Erythema Migrans
NCT03980015Not specifiedCOMPLETEDInflammatory Responses in Solitary and Multiple Erythema Migrans

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
DOXYCYCLINE ANHYDROUS46
AMOXICILLIN41
CEFUROXIME AXETIL41
PENICILLIN V41
1701