Fetal parvovirus syndrome
General Information (adopted from Orphanet):
| Synonyms, Signs: |
Parvovirus antenatal infection |
| Number of Symptoms | 9 |
| OrphanetNr: | 295 |
| 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: | No data available. |
| 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 Teratogenic Pierre Robin syndrome -Rare developmental defect during embryogenesis -Rare genetic disease -Rare maxillo-facial surgical disease -Rare otorhinolaryngologic disease |
Symptom Information:
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(HPO:0000478) | Abnormality of the eye | Occasional [Orphanet] | 126 / 7739 | |||
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(HPO:0010880) | Increased nuchal translucency | Occasional [Orphanet] | 13 / 7739 | |||
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(HPO:0001789) | Hydrops fetalis | Very frequent [Orphanet] | 63 / 7739 | |||
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(HPO:0001541) | Ascites | Very frequent [Orphanet] | 94 / 7739 | |||
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(HPO:0001511) | Intrauterine growth retardation | Occasional [Orphanet] | 358 / 7739 | |||
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(HPO:0001638) | Cardiomyopathy | Occasional [Orphanet] | 192 / 7739 | |||
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(HPO:0001903) | Anemia | Very frequent [Orphanet] | 289 / 7739 | |||
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(HPO:0001873) | Thrombocytopenia | Very frequent [Orphanet] | 224 / 7739 | |||
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(HPO:0001522) | Death in infancy | Occasional [Orphanet] | 275 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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