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General Information
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| Term |
Zika virus congenital syndrome |
ID (Ontology) |
DOID:0080180 (Human Disease) |
| Definition |
A syndrome that is characterized in neonates by microcephaly, craniofacial disproportion, spasticity, seizures, irritability and brainstem dysfunction including feeding difficulties, ocular abnormalities and findings on neuroimaging such as calcifications, cortical disorders and ventriculomegaly and has_material_basis_in the acquisition of Zika virus (Orthoflavivirus zikaense) infection in utero. |
| Also Known As |
"congenital Zika syndrome" ; "ZIKV congenital infection" |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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| Data Class | Field | Records |
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| Alleles (FBal) | HUMAN_DISEASE_INTERACTIONS | 7 | | Human Disease Models (FBhh) | DOID | 2 |
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Alleles | Genes | Human Disease Models |
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Zika virus congenital syndrome | 7 | 7 | 2 | model of | Zika virus congenital syndrome | 7 | -- | -- |
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Relationships