Ankyloglossia

Symptom Information:

Symptom ID: HPO:0010296
Synonyms:
Tongue tie [HPO:0010296]
Tongue tie (disorder) [Orphanet:10490]
Tongue tie [Orphanet:10490]
Ankyloglossia [OMIM:Ankyloglossia]
Ankyloglossia/lingual synechiae [Orphanet:10490]
Ankyloglossia congenital [Orphanet:10490]
Ankyloglossia congenital [MedDRA:10049244]
Congenital adhesions of tongue [MedDRA:10049244]
Congenital tongue adhesions [MedDRA:10049244]
Congenital tongue adhesions NOS [MedDRA:10049244]
Tongue tie [MedDRA:10049244]
Quality:
Cross references:
Orphanet:10490 "Ankyloglossia/lingual synechiae" [Orphanet:10490]
OMIM: "Ankyloglossia" [OMIM:Ankyloglossia]
UMLS:C0152415 "Ankyloglossia" [HPO:0010296]
UMLS:C0152415 "Tongue tie" [Orphanet:10490]
Is a (Direct Parents):
Orphanet Abnormality of the tongue
HPO         Abnormality of oral frenula
HPO         Abnormality of the tongue
MedDRA Tongue disorders
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 the tongue(HPO:0000157)
                         Ankyloglossia(HPO:0010296)
                      Abnormality of oral frenula(HPO:0000190)
                         Ankyloglossia(HPO:0010296)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Tongue conditions(MedDRA:10043946)
       Tongue disorders(MedDRA:10043954)
          Ankyloglossia(HPO:0010296)
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

1q21.1 microdeletion syndrome (Orphanet:250989)
ANKYLOGLOSSIA (OMIM:106280)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Catel-Manzke syndrome (Orphanet:1388)
Distal 22q11.2 microdeletion syndrome (Orphanet:261330)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Osteocraniostenosis (Orphanet:2763)
Recessive dystrophic epidermolysis bullosa inversa (Orphanet:79409)
Recessive dystrophic epidermolysis bullosa-generalized other (Orphanet:89842)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
X-linked cleft palate and ankyloglossia (Orphanet:324601)