Ehlers-Danlos syndrome, periodontitis type
MeSH: C562626ORPHA: 75392
Overview
Ehlers-Danlos syndromes (EDS) form a heterogeneous group of hereditary connective tissue diseases characterized by joint hyperlaxity, cutaneous hyperelasticity and tissue fragility
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with Ehlers-Danlos syndrome, periodontitis type, sourced from HPO and Orphanet clinical annotations.
Joint hypermobilityPeriodontitisHypermelanotic maculeAtrophic scarsShort statureGingival overgrowthMicrodontiaHyperextensible skinAtrophy of alveolar ridgesAgenesis of permanent teethMicrognathiaPremature loss of primary teeth
Classification & Codes
MeSH Code
C562626Orphanet Code
ORPHA:75392Ehlers-Danlos syndrome, periodontitis type
| MeSH | C562626 |
| Orphanet | ORPHA:75392 |
| Treatments | 0 drug(s) |
| Symptoms on record | 12 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO