Single median maxillary incisor
Symptom Information:
Symptom ID: | HPO:0006315 | ||||||||||||
Synonyms: |
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Quality: | |||||||||||||
Cross references: |
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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) Abnormality of the incisor(HPO:0000676) Abnormal number of incisors(HPO:0011064) Single median maxillary incisor(HPO:0006315) Abnormal number of teeth(HPO:0006483) Abnormal number of incisors(HPO:0011064) Single median maxillary incisor(HPO:0006315) MedDRA: |
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Database Frequency: | 13 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
16q24.3 microdeletion syndrome | (Orphanet:261250) |
19q13.11 microdeletion syndrome | (Orphanet:217346) |
Acrofacial dysostosis, Weyers type | (Orphanet:952) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
HOLOPROSENCEPHALY 2 | (OMIM:157170) |
HOLOPROSENCEPHALY 7 | (OMIM:610828) |
HOLOPROSENCEPHALY 9 | (OMIM:610829) |
Holoprosencephaly | (Orphanet:2162) |
Microform holoprosencephaly | (Orphanet:280200) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Solitary median maxillary central incisor syndrome | (Orphanet:2286) |
Thumb deformity - alopecia - pigmentation anomaly | (Orphanet:2251) |
WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME | (OMIM:602418) |