Selective tooth agenesis

Symptom Information:

Symptom ID: HPO:0001592
Synonyms:
Selective tooth agenesis [OMIM:Selective tooth agenesis]
Selective tooth agenesis (in some patients) [OMIM:Selective tooth agenesis (in some patients)]
Quality:
Cross references:
OMIM: "Selective tooth agenesis" [OMIM:Selective tooth agenesis]
OMIM: "Selective tooth agenesis (in some patients)" [OMIM:Selective tooth agenesis (in some patients)]
Is a (Direct Parents):
HPO         Agenesis of canine
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)
                               Selective tooth agenesis(HPO:0001592)
MedDRA:
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis (OMIM:615821)
Deafness - onychodystrophy (Orphanet:3231)
Deafness - onychodystrophy, autosomal dominant (Orphanet:79499)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
EEM syndrome (Orphanet:1897)
Frontometaphyseal dysplasia (Orphanet:1826)
Hallermann-Streiff syndrome (Orphanet:2108)
OCULODENTODIGITAL DYSPLASIA (OMIM:164200)
Oculodentodigital dysplasia (Orphanet:2710)
Otopalatodigital syndrome type 1 (Orphanet:90650)
SECKEL SYNDROME 1 (OMIM:210600)
Seckel syndrome (Orphanet:808)
TOOTH AGENESIS, SELECTIVE, 6 (OMIM:613097)