Periodontitis

Symptom Information:

Symptom ID: HPO:0000704
Synonyms:
Periodontal disease [HPO:0000704]
Periodontitis (disorder) [Orphanet:12950]
Pericementitis [Orphanet:12950]
Periodontitis [Orphanet:12950]
Periodontal disease [OMIM:Periodontal disease]
Periodontitis [OMIM:Periodontitis]
Alveolysis/paraodontitis [Orphanet:12950]
Periodontitis [MedDRA:10034539]
Acute apical periodontitis of pulpal origin [MedDRA:10034539]
Acute periodontitis [MedDRA:10034539]
Chronic apical periodontitis [MedDRA:10034539]
Chronic periodontitis [MedDRA:10034539]
Periodontal infection [MedDRA:10034539]
Periodontosis [MedDRA:10034539]
Pyorrhea [MedDRA:10034539]
Pyorrhoea [MedDRA:10034539]
Pericementitis [MedDRA:10034539]
Acute apical periodontitis [MedDRA:10034539]
Periodontosis [OMIM:Periodontosis]
Alveolysis [Orphanet:12950]
Periodontal disease [MedDRA:10034536]
Quality:
Cross references:
Orphanet:12950 "Alveolysis/paraodontitis" [Orphanet:12950]
OMIM: "Periodontal disease" [OMIM:Periodontal disease]
OMIM: "Periodontitis" [OMIM:Periodontitis]
OMIM: "Periodontosis" [OMIM:Periodontosis]
UMLS:C0031099 "Periodontitis" [HPO:0000704]
UMLS:C0031051 "Pericementitis" [Orphanet:12950]
UMLS:C0031099 "Periodontitis" [Orphanet:12950]
Is a (Direct Parents):
HPO         Abnormality of the teeth
HPO         Abnormality of the gingiva
MedDRA Dental and oral soft tissue infections
Orphanet Abnormality of the teeth
MedDRA Dental disorders NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the mouth(HPO:0000153)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of the teeth(HPO:0000164)
                         Periodontitis(HPO:0000704)
                      Abnormality of the gingiva(HPO:0000168)
                         Periodontitis(HPO:0000704)
MedDRA:
Infections and infestations(MedDRA:10021881)
    Infections - pathogen unspecified(MedDRA:10021879)
       Dental and oral soft tissue infections(MedDRA:10012326)
          Periodontitis(HPO:0000704)
Gastrointestinal disorders(MedDRA:10017947)
    Dental and gingival conditions(MedDRA:10044018)
       Dental disorders NEC(MedDRA:10044037)
          Periodontitis(HPO:0000704)
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

Acroosteolysis, dominant type (Orphanet:955)
Alopecia - epilepsy - pyorrhea - intellectual deficit (Orphanet:1008)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 10 (OMIM:615987)
Chédiak-Higashi syndrome (Orphanet:167)
Cyclic neutropenia (Orphanet:2686)
Ehlers-Danlos syndrome, periodontitis type (Orphanet:75392)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Geroderma osteodysplastica (Orphanet:2078)
Haim-Munk syndrome (Orphanet:2342)
Hereditary acrokeratotic poikiloderma of Kindler-Weary (Orphanet:306539)
Hermansky-Pudlak syndrome with neutropenia (Orphanet:183678)
Hypoplasminogenemia (Orphanet:722)
Kindler syndrome (Orphanet:2908)
Leukocyte adhesion deficiency (Orphanet:2968)
Leukocyte adhesion deficiency type I (Orphanet:99842)
Leukocyte adhesion deficiency type II (Orphanet:99843)
Ligneous conjunctivitis (Orphanet:97231)
NEUTROPENIA, CHRONIC FAMILIAL (OMIM:162700)
Neutropenia, severe congenital, 1, autosomal dominant (OMIM:202700)
Oculocerebrorenal syndrome (Orphanet:534)
PERIODONTITIS, CHRONIC (OMIM:260950)
Papillon-Lefèvre syndrome (Orphanet:678)