Abnormality of the oral cavity

Symptom Information:

Symptom ID: HPO:0000163
Cross references:
Is a (Direct Parents):
HPO         Oral cavity bleeding
HPO         Oral bleeding
HPO         Abnormality of the mouth
Is a (Whole tree): HPO:
    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)
Database Frequency: 37 / 7739

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)