Summary Literature (0)

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 :

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0010284 - Armfield syndrome

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee