Anodontia
Symptom Information:
Symptom ID: | HPO:0000674 | |||||||||||
Synonyms: |
|
|||||||||||
Quality: | ||||||||||||
Cross references: |
|
|||||||||||
Is a (Direct Parents): |
|
|||||||||||
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) |