Ehlers-Danlos syndrome, periodontitis type
Ehlers-Danlos syndromes (EDS) form a heterogeneous group of hereditary connective tissue diseases characterized by joint hyperlaxity, cutaneous hyperelasticity and tissue fragility
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Ehlers-Danlos syndrome, periodontitis type
Summary
Ehlers-Danlos syndrome, periodontitis type is a developmental defect during embryogenesis[1].
Key Facts
- Ehlers-Danlos syndrome, periodontitis type's instance of is recorded as developmental defect during embryogenesis[2].
- Ehlers-Danlos syndrome, periodontitis type's instance of is recorded as rare disease[3].
- Ehlers-Danlos syndrome, periodontitis type's instance of is recorded as class of disease[4].
- Ehlers-Danlos syndrome, periodontitis type is a type of rare disease with odontological manifestation[5].
- Ehlers-Danlos syndrome, periodontitis type is a type of Ehlers-Danlos syndrome[6].
- Ehlers-Danlos syndrome, periodontitis type's genetic association is recorded as C1R[7].
- Ehlers-Danlos syndrome, periodontitis type's genetic association is recorded as C1S[8].
- Ehlers-Danlos syndrome, periodontitis type's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_75392[9].