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General Information
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| Term |
mandibulofacial dysostosis, Guion-Almeida type |
ID (Ontology) |
DOID:0080196 (Human Disease) |
| Definition |
A syndrome characterized by progressive microcephaly, micrognathia, microtia, dysplastic ears, preauricular skin tags, speech delay, significant developmental delay, midface and malar hypoplasia. |
| Also Known As |
"mandibulofacial dysostosis with microcephaly" ; "mandibulofacial dysostosis-microcephaly syndrome" ; "MFDM syndrome" |
| 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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No relevant records available
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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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| Genes |
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mandibulofacial dysostosis, Guion-Almeida type | 1 | for disease ribbon | mandibulofacial dysostosis, Guion-Almeida type | 1 | model of | mandibulofacial dysostosis, Guion-Almeida type | 1 |
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Relationships