Fetal varicella syndrome
General Information (adopted from Orphanet):
Synonyms, Signs: |
Varicella virus antenatal infection |
Number of Symptoms | 8 |
OrphanetNr: | 291 |
OMIM Id: |
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ICD-10: |
P35.8 |
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: | > 100 cases [Orphanet] |
Inheritance: |
Not applicable [Orphanet] |
Age of onset: |
Antenatal Neonatal [Orphanet] |
Disease classification (adopted from Orphanet):
Parent Diseases: |
Infectious embryofetopathy
-Rare developmental defect during embryogenesis -Rare infectious disease |
Symptom Information:
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(HPO:0000252) | Microcephaly | Frequent [Orphanet] | 832 / 7739 | |||
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(HPO:0008056) | Aplasia/Hypoplasia affecting the eye | Frequent [Orphanet] | 142 / 7739 | |||
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(HPO:0000518) | Cataract | Frequent [Orphanet] | 454 / 7739 | |||
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(HPO:0002983) | Micromelia | Frequent [Orphanet] | 130 / 7739 | |||
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(HPO:0001511) | Intrauterine growth retardation | Very frequent [Orphanet] | 358 / 7739 | |||
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(HPO:0000987) | Atypical scarring of skin | Very frequent [Orphanet] | 58 / 7739 | |||
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(HPO:0012758) | Neurodevelopmental delay | Frequent [Orphanet] | 949 / 7739 | |||
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(HPO:0002120) | Cerebral cortical atrophy | Frequent [Orphanet] | 187 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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