Abnormality of the oral cavity
Symptom Information:
| Symptom ID: | HPO:0000163 | ||||||
| Synonyms: |
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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) MedDRA: |
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| Database Frequency: | 37 / 7739 | ||||||
| Resource: |
All diseases associated with this symptom:
| Acrodermatitis enteropathica, zinc deficiency type | (Orphanet:37) |
| Alopecia - epilepsy - pyorrhea - intellectual deficit | (Orphanet:1008) |
| Autosomal dominant striatal neurodegeneration | (Orphanet:228169) |
| Autosomal recessive multiple pterygium syndrome | (Orphanet:2990) |
| Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
| Choreoacanthocytosis | (Orphanet:2388) |
| Desmosterolosis | (Orphanet:35107) |
| Dyskeratosis congenita | (Orphanet:1775) |
| Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
| Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
| Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
| Ellis Van Creveld syndrome | (Orphanet:289) |
| Eosinophilic granuloma | (Orphanet:99871) |
| Flat face - microstomia - ear anomaly | (Orphanet:1968) |
| Focal palmoplantar and gingival keratoderma | (Orphanet:2200) |
| Gamma heavy-chain disease | (Orphanet:100026) |
| Hallermann-Streiff syndrome | (Orphanet:2108) |
| Heart defect - round face - congenital developmental delay | (Orphanet:1355) |
| Hennekam syndrome | (Orphanet:2136) |
| Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
| Hypoplasminogenemia | (Orphanet:722) |
| Intellectual deficit - microcephaly - phalangeal - facial abnormalities | (Orphanet:3067) |
| KID syndrome | (Orphanet:477) |
| Lipoid proteinosis | (Orphanet:530) |
| Malakoplakia | (Orphanet:556) |
| Multiple endocrine neoplasia type 2 | (Orphanet:653) |
| Mutilating palmoplantar keratoderma with periorificial keratotic plaques | (Orphanet:659) |
| Odonto-onycho-dermal dysplasia | (Orphanet:2721) |
| Oral submucous fibrosis | (Orphanet:357154) |
| Orofaciodigital syndrome type 8 | (Orphanet:2755) |
| Pai syndrome | (Orphanet:1993) |
| Pityriasis rubra pilaris | (Orphanet:2897) |
| Progeria - short stature - pigmented nevi | (Orphanet:2959) |
| Retinopathy - anemia- central nervous system anomalies | (Orphanet:3088) |
| Scleroderma | (Orphanet:801) |
| Stüve-Wiedemann syndrome | (Orphanet:3206) |
| Tumoral calcinosis | (Orphanet:53715) |