Abnormality of oral mucosa

Symptom Information:

Symptom ID: HPO:0011830
Synonyms:
Oral mucosa anomaly [Orphanet:10000]
Anomalies of tongue, gingiva and oral mucosa [Orphanet:10000]
Quality:
Cross references:
Orphanet:10000 "Anomalies of tongue, gingiva and oral mucosa" [Orphanet:10000]
Is a (Direct Parents):
HPO         Enanthema
Orphanet Abnormality of the tongue
HPO         Abnormality of the oral cavity
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 oral mucosa(HPO:0011830)
MedDRA:
Database Frequency: 47 / 7739
Resource:

All diseases associated with this symptom:

Acquired epidermolysis bullosa (Orphanet:46487)
Behçet disease (Orphanet:117)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Bullous pemphigoid (Orphanet:703)
CINCA syndrome (Orphanet:1451)
Cogan syndrome (Orphanet:1467)
Cutaneous leukocytoclastic angiitis (Orphanet:889)
Cyclic neutropenia (Orphanet:2686)
Darier disease (Orphanet:218)
Drug rash with eosinophilia and systemic symptoms (Orphanet:139402)
Epidermolysis bullosa simplex with pyloric atresia (Orphanet:158684)
Epidermolysis bullosa simplex, Dowling-Meara type (Orphanet:79396)
Familial Mediterranean fever (Orphanet:342)
Familial benign chronic pemphigus (Orphanet:2841)
Generalized epidermolysis bullosa simplex, non-Dowling-Meara type (Orphanet:79399)
Granulomatosis with polyangiitis (Orphanet:900)
Hashimoto-Pritzker syndrome (Orphanet:99872)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Inherited epidermolysis bullosa (Orphanet:79361)
Junctional epidermolysis bullosa, Herlitz type (Orphanet:79404)
Juvenile xanthogranuloma (Orphanet:158000)
KID syndrome (Orphanet:477)
Kawasaki disease (Orphanet:2331)
Lethal acantholytic epidermolysis bullosa (Orphanet:158687)
Linear IgA dermatosis (Orphanet:46488)
Lyell syndrome (Orphanet:537)
Marshall syndrome with periodic fever (Orphanet:42642)
Methylmalonic acidemia with homocystinuria (Orphanet:26)
Methylmalonic acidemia with homocystinuria, type cblF (Orphanet:79284)
Muckle-Wells syndrome (Orphanet:575)
Mucous membrane pemphigoid (Orphanet:46486)
Multicentric reticulohistiocytosis (Orphanet:139436)
Pachyonychia congenita (Orphanet:2309)
Paraneoplastic pemphigus (Orphanet:63455)
Pemphigus vulgaris (Orphanet:704)
Reactive arthritis (Orphanet:29207)
Recessive dystrophic epidermolysis bullosa-generalized other (Orphanet:89842)
Relapsing polychondritis (Orphanet:728)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Shwachman-Diamond syndrome (Orphanet:811)
Stevens-Johnson syndrome (Orphanet:36426)
Sweet syndrome (Orphanet:3243)
TRAPS syndrome (Orphanet:32960)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
Xanthoma disseminatum (Orphanet:158003)