Abnormality of oral mucosa
Symptom Information:
Symptom ID: | HPO:0011830 | ||||||
Synonyms: |
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Quality: | |||||||
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 oral mucosa(HPO:0011830) MedDRA: |
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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) |