has material basis in germline mutation in FAM50A syndromic disease hereditary disease Armfield syndrome https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/armfield_syndrome https://www.malacards.org/card/intellectual_developmental_disorder_x_linked_syndromic_armfield_type UMLS:C1846057 mental retardation, X-linked, syndromic, Armfield type Orphanet:85276 mental retardation syndrome, X-linked, armfield type, X-linked recessive syndromic X-linked intellectual disability Armfield type Armfield X-linked intellectual disability syndrome X-linked intellectual disability, Armfield type MESH:C564551 Armfield X-linked mental retardation syndrome GARD:0016742 MONDO:0010284 OMIM:300261 MRXSA SCTID:719017003 intellectual developmental disorder, X-linked, syndromic, Armfield type, X-linked recessive Armfield syndrome DOID:0050764 MEDGEN:375800 intellectual disability syndrome, X-linked, Armfield type X-linked intellectual disability, Armfield type is characterized by intellectual deficiency, short stature, seizures, and small hands and feet. It has been described in six males from three generations of one family. Three of them also had cataracts/glaucoma and two of them had cleft palate. The locus has been mapped to the terminal 8 Mb of Xq28. multiple congenital anomalies/dysmorphic syndrome-intellectual disability X-linked syndromic intellectual disability