Anodontia

Symptom Information:

Symptom ID: HPO:0000674
Synonyms:
Dental agenesis [HPO:0000674]
Complete congenital absence of teeth [HPO:0000674]
Anodontia (disorder) [Orphanet:12300]
Complete congenital absence of teeth (disorder) [Orphanet:12300]
Developmental absence of tooth [Orphanet:12300]
Anodontia [OMIM:Anodontia]
Dental agenesis [OMIM:Dental agenesis]
Anodontia/oligodontia/hypodontia [Orphanet:12300]
Anodontia [Orphanet:12300]
Anodontia [MedDRA:10002583]
Anodontia (in some patients) [OMIM:Anodontia (in some patients)]
Quality:
Cross references:
Orphanet:12300 "Anodontia/oligodontia/hypodontia" [Orphanet:12300]
OMIM: "Anodontia" [OMIM:Anodontia]
OMIM: "Dental agenesis" [OMIM:Dental agenesis]
OMIM: "Anodontia (in some patients)" [OMIM:Anodontia (in some patients)]
UMLS:C1504306 "Anodontia" [HPO:0000674]
UMLS:C0399352 "Developmental absence of tooth" [Orphanet:12300]
Is a (Direct Parents):
Orphanet Hypodontia
Orphanet Abnormality of the teeth
MedDRA Agenesis of permanent teeth
HPO         Reduced number of teeth
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 teeth(HPO:0000164)
                         Abnormal number of teeth(HPO:0006483)
                            Reduced number of teeth(HPO:0009804)
                               Anodontia(HPO:0000674)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Dental and gingival conditions(MedDRA:10044018)
       Agenesis of permanent teeth(HPO:0006349)
          Anodontia(HPO:0000674)
Database Frequency: 18 / 7739
Resource:

All diseases associated with this symptom:

AREDYLD syndrome (Orphanet:1133)
Acro-oto-ocular syndrome (Orphanet:2980)
Anodontia (Orphanet:99797)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
Bloom syndrome (Orphanet:125)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT (OMIM:129490)
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE (OMIM:224900)
Oculoosteocutaneous syndrome (Orphanet:2713)
Rosselli-Gulienetti syndrome (Orphanet:90339)
TELECANTHUS (OMIM:187350)
Tricho-odonto-onychial dysplasia (Orphanet:3355)
VAN DER WOUDE SYNDROME 2 (OMIM:606713)
Wilson-Turner syndrome (Orphanet:3459)
Woodhouse-Sakati syndrome (Orphanet:3464)
Zlotogora-Ogur syndrome (Orphanet:3253)