Fibrous syngnathia

Symptom Information:

Symptom ID: HPO:0009754
Synonyms:
Fusion of the alveolar ridges [HPO:0009754]
Syngnathia [HPO:0009754]
Syngnathia [OMIM:Syngnathia]
Quality:
Cross references:
OMIM: "Syngnathia" [OMIM:Syngnathia]
UMLS:C1861546 "Syngnathia" [HPO:0009754]
Is a (Direct Parents):
HPO         Abnormality of the mandible
HPO         Abnormality of the alveolar ridges
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 skull(HPO:0000929)
                Abnormality of facial skeleton(HPO:0011821)
                   Abnormality of the mandible(HPO:0000277)
                      Fibrous syngnathia(HPO:0009754)
             Abnormality of the face(HPO:0000271)
                Abnormality of the mouth(HPO:0000153)
                   Abnormality of the oral cavity(HPO:0000163)
                      Abnormality of the alveolar ridges(HPO:0006477)
                         Fibrous syngnathia(HPO:0009754)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the skull(HPO:0000929)
                   Abnormality of facial skeleton(HPO:0011821)
                      Abnormality of the mandible(HPO:0000277)
                         Fibrous syngnathia(HPO:0009754)
MedDRA:
Database Frequency: 1 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant popliteal pterygium syndrome (Orphanet:1300)