Nasal dermoid cyst
General Information (adopted from Orphanet):
Synonyms, Signs: |
Nasal dermoid sinus cyst |
Number of Symptoms | 16 |
OrphanetNr: | 141103 |
OMIM Id: |
600679
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ICD-10: |
Q18.8 |
UMLs: |
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MeSH: |
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MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
Autosomal dominant inheritance [Omim] |
Age of onset: |
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Disease classification (adopted from Orphanet):
Parent Diseases: |
Cysts and fistulae of the face and oral cavity
-Rare developmental defect during embryogenesis -Rare genetic disease -Rare otorhinolaryngologic disease |
Symptom Information:
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(HPO:0000458) | Anosmia | 49 / 7739 | ||||
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(HPO:0000431) | Wide nasal bridge | 290 / 7739 | ||||
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(HPO:0001742) | Nasal obstruction | 5 / 7739 | ||||
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(HPO:0000316) | Hypertelorism | 644 / 7739 | ||||
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(HPO:0004411) | Deviated nasal septum | 3 / 7739 | ||||
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(HPO:0001085) | Papilledema | 31 / 7739 | ||||
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(HPO:0001250) | Seizures | 1245 / 7739 | ||||
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(HPO:0000751) | Personality changes | 33 / 7739 | ||||
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(HPO:0002357) | Dysphasia | 33 / 7739 | ||||
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(HPO:0000951) | Abnormality of the skin | 147 / 7739 | ||||
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(OMIM) | Anterior clinoid erosion | 1 / 7739 | ||||
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(OMIM) | Infraglabellar dermal sinuses | 1 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 | ||||
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(OMIM) | Nocturnal seizures with hallucinations and postictal dysphasia | 1 / 7739 | ||||
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(OMIM) | Widened nasal septum, and an avascular mass arising from the cribriform plate | 1 / 7739 | ||||
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(OMIM) | Frontonasal dermoid cysts | 1 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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