Pituitary dermoid and epidermoid cysts
General Information (adopted from Orphanet):
Synonyms, Signs: |
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Number of Symptoms | 2 |
OrphanetNr: | 91351 |
OMIM Id: |
131600
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ICD-10: |
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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: |
Adrenal/paraganglial tumor
-Rare endocrine disease -Rare oncologic disease Pituitary hormone deficiency from tumoral origin -Rare endocrine disease -Rare genetic disease |
Symptom Information:
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(HPO:0200040) | Epidermoid cyst | 35 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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