Oral synechia
Symptom Information:
Symptom ID: | HPO:0010285 | ||||
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) Oral synechia(HPO:0010285) MedDRA: |
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Database Frequency: | 31 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Acrofacial dysostosis, Weyers type | (Orphanet:952) |
Autosomal dominant popliteal pterygium syndrome | (Orphanet:1300) |
Bohring-Opitz syndrome | (Orphanet:97297) |
C syndrome | (Orphanet:1308) |
Cataract - aberrant oral frenula - growth delay | (Orphanet:1373) |
Cleft palate-lateral synechia syndrome | (Orphanet:2016) |
Craniofacial dyssynostosis | (Orphanet:1516) |
Deafness-craniofacial syndrome | (Orphanet:3241) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome type 2 | (Orphanet:90318) |
Ehlers-Danlos syndrome, vascular type | (Orphanet:286) |
Ellis Van Creveld syndrome | (Orphanet:289) |
Grix-Blankenship-Peterson syndrome | (Orphanet:2099) |
Joubert syndrome with hepatic defect | (Orphanet:1454) |
Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
Kallmann syndrome - heart disease | (Orphanet:2326) |
Lacrimo-auriculo-dento-digital syndrome | (Orphanet:2363) |
Mandibulofacial dysostosis-microcephaly syndrome | (Orphanet:79113) |
Mesomelia-synostoses syndrome | (Orphanet:2496) |
Orofaciodigital syndrome type 1 | (Orphanet:2750) |
Orofaciodigital syndrome type 10 | (Orphanet:2756) |
Orofaciodigital syndrome type 4 | (Orphanet:2753) |
Orofaciodigital syndrome type 5 | (Orphanet:2919) |
Orofaciodigital syndrome type 8 | (Orphanet:2755) |
Pai syndrome | (Orphanet:1993) |
Pallister-Hall syndrome | (Orphanet:672) |
Recombinant 8 syndrome | (Orphanet:96167) |
Renal-genital-middle ear anomalies | (Orphanet:1092) |
Short stature - heart defect - craniofacial anomalies | (Orphanet:1088) |
Syngnathia multiple anomalies | (Orphanet:3262) |
Trisomy 8q | (Orphanet:1752) |