Oral synechia

Symptom Information:

Symptom ID: HPO:0010285
Oral synechiae/abnormal frenulae [Orphanet:10630]
Cross references:
Orphanet:10630 "Oral synechiae/abnormal frenulae" [Orphanet:10630]
Is a (Direct Parents):
Orphanet Abnormality of the tongue
HPO         Abnormality of oral mucosa
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)
                      Abnormality of oral mucosa(HPO:0011830)
                         Oral synechia(HPO:0010285)
Database Frequency: 31 / 7739

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)