Gingivitis
Symptom Information:
Symptom ID: | HPO:0000230 | |||||||
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) Gingivitis(HPO:0000230) MedDRA: Infections and infestations(MedDRA:10021881) Infections - pathogen unspecified(MedDRA:10021879) Dental and oral soft tissue infections(MedDRA:10012326) Gingivitis(HPO:0000230) |
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Database Frequency: | 31 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Alopecia - epilepsy - pyorrhea - intellectual deficit | (Orphanet:1008) |
Alström syndrome | (Orphanet:64) |
Autosomal dominant hyper-IgE syndrome | (Orphanet:2314) |
Chronic granulomatous disease | (Orphanet:379) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Cyclic neutropenia | (Orphanet:2686) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Ehlers-Danlos syndrome, progeroid type | (Orphanet:75496) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
GOLGI REASSEMBLY STACKING PROTEIN 1 | (OMIM:606867) |
Hartnup syndrome | (Orphanet:2116) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Hurler syndrome | (Orphanet:93473) |
Hypoplasminogenemia | (Orphanet:722) |
Kindler syndrome | (Orphanet:2908) |
Kostmann syndrome | (Orphanet:99749) |
Leukocyte adhesion deficiency | (Orphanet:2968) |
Leukocyte adhesion deficiency type I | (Orphanet:99842) |
Mucous membrane pemphigoid | (Orphanet:46486) |
NEUTROPENIA, CHRONIC FAMILIAL | (OMIM:162700) |
Neutropenia, severe congenital, 1, autosomal dominant | (OMIM:202700) |
Normocalcemic tumoral calcinosis | (Orphanet:306658) |
Oculocerebrorenal syndrome | (Orphanet:534) |
PACHYONYCHIA CONGENITA 3 | (OMIM:615726) |
Papillon-Lefèvre syndrome | (Orphanet:678) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Scleroderma | (Orphanet:801) |
Stern-Lubinsky-Durrie syndrome | (Orphanet:3194) |
Tuberous sclerosis | (Orphanet:805) |
Tumoral calcinosis | (Orphanet:53715) |
X-linked hyper-IgM syndrome | (Orphanet:101088) |