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General Information
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| Term |
Armfield syndrome |
ID (Ontology) |
DOID:0050764 (Human Disease) |
| Definition |
A syndromic X-linked intellectual disability characterized by intellectual disability, short stature, seizures, and small hands and feet and in some cases cleft palate or cataracts/glaucoma that has_material_basis_in variation in the chromosomal region Xq28. |
| Also Known As |
"Armfield X-linked mental retardation syndrome" ; "mental retardation syndrome, X-linked, Armfield type" ; "MRXSA" (for all, see Synonyms field below) |
| 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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Armfield syndrome | 1 | for disease ribbon | Armfield syndrome | 1 | model of | Armfield syndrome | 1 |
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Relationships