Widely-spaced maxillary central incisors
Symptom Information:
Symptom ID: | HPO:0001566 | |||||||||||
Synonyms: |
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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) Misalignment of incisors(HPO:0011062) Widely-spaced incisors(HPO:0006304) Widely-spaced maxillary central incisors(HPO:0001566) Misalignment of teeth(HPO:0000692) Diastema(HPO:0000699) Widely-spaced maxillary central incisors(HPO:0001566) Misalignment of incisors(HPO:0011062) Widely-spaced incisors(HPO:0006304) Widely-spaced maxillary central incisors(HPO:0001566) MedDRA: |
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Database Frequency: | 15 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
Atkin-Flaitz syndrome | (Orphanet:1193) |
CLARK-BARAITSER SYNDROME | (OMIM:300602) |
Carpenter-Waziri syndrome | (Orphanet:93973) |
Cataract-congenital heart disease-neural tube defect syndrome | (Orphanet:314993) |
Chudley-Lowry-Hoar syndrome | (Orphanet:93971) |
DIASTEMA, DENTAL MEDIAL | (OMIM:125900) |
Frontonasal dysplasia | (Orphanet:250) |
Holmes-Gang syndrome | (Orphanet:93970) |
Juberg-Marsidi syndrome | (Orphanet:93972) |
KBG syndrome | (Orphanet:2332) |
MMEP syndrome | (Orphanet:3434) |
Renier-Gabreels-Jasper syndrome | (Orphanet:93975) |
Smith-Fineman-Myers syndrome | (Orphanet:93974) |
X-linked intellectual deficit - hypotonic face | (Orphanet:73220) |