Fetal cytomegalovirus syndrome
General Information (adopted from Orphanet):
| Synonyms, Signs: |
CMV antenatal infection Cytomegalovirus antenatal infection |
| Number of Symptoms | 6 |
| OrphanetNr: | 294 |
| OMIM Id: |
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| ICD-10: |
P35.1 |
| UMLs: |
C0349499 |
| MeSH: |
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| MedDRA: |
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| Snomed: |
276701009 |
Prevalence, inheritance and age of onset:
| Prevalence: | 40 of 100 000 [Orphanet] |
| Inheritance: |
Not applicable [Orphanet] |
| Age of onset: |
Neonatal Infancy [Orphanet] |
Disease classification (adopted from Orphanet):
| Parent Diseases: |
Infectious disease with epilepsy
-Rare neurologic disease Infectious embryofetopathy -Rare developmental defect during embryogenesis -Rare infectious disease |
Symptom Information:
|
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(HPO:0000478) | Abnormality of the eye | Very frequent [Orphanet] | 126 / 7739 | |||
|
|
(HPO:0000407) | Sensorineural hearing impairment | Very frequent [Orphanet] | 524 / 7739 | |||
|
|
(HPO:0002240) | Hepatomegaly | Frequent [Orphanet] | 467 / 7739 | |||
|
|
(HPO:0001744) | Splenomegaly | Frequent [Orphanet] | 337 / 7739 | |||
|
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(HPO:0001903) | Anemia | Frequent [Orphanet] | 289 / 7739 | |||
|
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(HPO:0001928) | Abnormality of coagulation | Frequent [Orphanet] | 44 / 7739 |
Associated genes:
ClinVar (via SNiPA)
| Gene symbol | Variation | Clinical significance | Reference |
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