Agenesis of permanent teeth

Symptom Information:

Symptom ID: HPO:0006349
Synonyms:
Absence of permanent teeth [HPO:0006349]
Absent permanent teeth [HPO:0006349]
Missing teeth [HPO:0006349]
Absent permanent teeth [OMIM:Absent permanent teeth]
Missing teeth [OMIM:Missing teeth]
Tooth missing [MedDRA:10044048]
Quality:
Cross references:
OMIM: "Absent permanent teeth" [OMIM:Absent permanent teeth]
OMIM: "Missing teeth" [OMIM:Missing teeth]
Is a (Direct Parents):
HPO         Abnormal number of permanent teeth
HPO         Reduced number of teeth
MedDRA Dental and gingival conditions
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)
                            Abnormal number of permanent teeth(HPO:0011044)
                               Agenesis of permanent teeth(HPO:0006349)
                            Reduced number of teeth(HPO:0009804)
                               Agenesis of permanent teeth(HPO:0006349)
MedDRA:
Gastrointestinal disorders(MedDRA:10017947)
    Dental and gingival conditions(MedDRA:10044018)
       Agenesis of permanent teeth(HPO:0006349)
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

Alström syndrome (Orphanet:64)
CARPENTER SYNDROME 1 (OMIM:201000)
Carpenter syndrome (Orphanet:65759)
Cerebellar ataxia - ectodermal dysplasia (Orphanet:1174)
Dubowitz syndrome (Orphanet:235)
Fried's tooth and nail syndrome (Orphanet:99672)
Hypodontia - dysplasia of nails (Orphanet:2228)
Johanson-Blizzard syndrome (Orphanet:2315)
Oculotrichodysplasia (Orphanet:2718)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Rothmund-Thomson syndrome (Orphanet:2909)
Scalp-ear-nipple syndrome (Orphanet:2036)