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DOID:0050764 - Armfield syndrome
Disease Ontology 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.
Synonyms: Armfield X-linked mental retardation syndrome, mental retardation syndrome, X-linked, Armfield type, MRXSA, syndromic X-linked mental retardation Armfield type, X-linked intellectual disability, Armfield type
Echinobase Genes
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Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee