Short lingual frenulum
Symptom Information:
Symptom ID: | HPO:0000200 | |||
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 oral frenula(HPO:0000190) Short lingual frenulum(HPO:0000200) MedDRA: |
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Database Frequency: | 4 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Autosomal dominant Opitz G/BBB syndrome | (Orphanet:306588) |
Deafness-craniofacial syndrome | (Orphanet:3241) |
Opitz G/BBB syndrome | (Orphanet:2745) |
Peters-plus syndrome | (Orphanet:709) |