Glossitis

Symptom Information:

Symptom ID: HPO:0000206
Synonyms:
Glossitis (disorder) [Orphanet:10560]
Glossitis [Orphanet:10560]
Glossitis [OMIM:Glossitis]
Glossitis [MedDRA:10018386]
Glossitis acute [MedDRA:10018386]
Inflammation tongue [MedDRA:10018386]
Median rhomboid glossitis [MedDRA:10018386]
Sore inflamed tongue [MedDRA:10018386]
Tongue inflammation [MedDRA:10018386]
Tongue irritation [MedDRA:10018386]
Tongue red swollen pain [MedDRA:10018386]
Raw tongue [MedDRA:10018386]
Tongue mucositis [MedDRA:10018386]
Quality:
Cross references:
Orphanet:10560 "Glossitis" [Orphanet:10560]
OMIM: "Glossitis" [OMIM:Glossitis]
UMLS:C0017675 "Glossitis" [HPO:0000206]
UMLS:C0017675 "Glossitis" [Orphanet:10560]
Is a (Direct Parents):
Orphanet Abnormality of the tongue
MedDRA Tongue disorders
HPO         Abnormality of the tongue
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 tongue(HPO:0000157)
                         Glossitis(HPO:0000206)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Tongue conditions(MedDRA:10043946)
       Tongue disorders(MedDRA:10043954)
          Glossitis(HPO:0000206)
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Acquired hypertrichosis lanuginosa (Orphanet:2221)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Cronkhite-Canada syndrome (Orphanet:2930)
Giant cell arteritis (Orphanet:397)
Hartnup syndrome (Orphanet:2116)
Hereditary folate malabsorption (Orphanet:90045)
Kawasaki disease (Orphanet:2331)
Methylmalonic acidemia with homocystinuria (Orphanet:26)
Methylmalonic acidemia with homocystinuria, type cblF (Orphanet:79284)