Periodontitis
Symptom Information:
Symptom ID: | HPO:0000704 | |||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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 gingiva(HPO:0000168) Periodontitis(HPO:0000704) Abnormality of the teeth(HPO:0000164) 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) |
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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) |