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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, MRXSA, X-linked intellectual disability, Armfield type, mental retardation syndrome, X-linked, Armfield type, syndromic X-linked mental retardation Armfield type,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0010284 - Armfield syndrome |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee