Gingivitis

Symptom Information:

Symptom ID: HPO:0000230
Synonyms:
Gingivitis (disorder) [Orphanet:10910]
Gingivitis [Orphanet:10910]
Gingivitis [OMIM:Gingivitis]
Gingivitis [MedDRA:10018292]
Acute gingivitis [MedDRA:10018292]
Chronic gingivitis [MedDRA:10018292]
Gingivitis aggravated [MedDRA:10018292]
Quality:
Cross references:
Orphanet:10910 "Gingivitis" [Orphanet:10910]
OMIM: "Gingivitis" [OMIM:Gingivitis]
UMLS:C0017574 "Gingivitis" [HPO:0000230]
UMLS:C0017574 "Gingivitis" [Orphanet:10910]
Is a (Direct Parents):
Orphanet Abnormality of the tongue
HPO         Abnormality of the gingiva
MedDRA Dental and oral soft tissue infections
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)
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)