Ptosis - vocal cord paralysis
General Information (adopted from Orphanet):
Synonyms, Signs:
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Tucker syndrome
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Number of Symptoms
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10
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OrphanetNr:
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2997
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OMIM Id:
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193240
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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:
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No data available.
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Inheritance:
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Autosomal dominant inheritance
[Omim]
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Age of onset:
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Disease classification (adopted from Orphanet):
Parent Diseases:
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Ptosis
-Rare eye disease
-Rare genetic disease
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1
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(HPO:0001488)
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Bilateral ptosis |
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|
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42 / 7739
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2
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(HPO:0000508)
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Ptosis |
Very frequent [Orphanet]
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|
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459 / 7739
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3
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(HPO:0001605)
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Vocal cord paralysis |
|
|
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13 / 7739
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4
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(HPO:0004374)
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Hemiplegia/hemiparesis |
Very frequent [Orphanet]
|
|
|
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158 / 7739
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5
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(HPO:0001622)
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Premature birth |
Frequent [Orphanet]
|
|
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100 / 7739
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6
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(HPO:0004322)
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Short stature |
Frequent [Orphanet]
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|
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1232 / 7739
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7
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(HPO:0001601)
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Laryngomalacia |
Very frequent [Orphanet]
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|
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61 / 7739
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8
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(HPO:0001608)
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Abnormality of the voice |
Very frequent [Orphanet]
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|
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126 / 7739
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9
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(HPO:0000006)
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Autosomal dominant inheritance |
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|
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2518 / 7739
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10
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(OMIM)
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Bilateral recurrent laryngeal nerve paralysis |
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1 / 7739
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ClinVar (via SNiPA)
Gene symbol |
Variation |
Clinical significance |
Reference |