Selective tooth agenesis
Symptom Information:
Symptom ID: | HPO:0001592 | ||||
Synonyms: |
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Is a (Direct Parents): |
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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: |
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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) |