syndromic disease Atkin-Flaitz syndrome https://www.malacards.org/card/atkin_flaitz_syndrome GARD:0003537 MEDGEN:163230 MESH:C538195 MONDO:0010323 Orphanet:1193 SCTID:718577005 UMLS:C0796206 Atkin-Flaitz syndrome OMIM:300431 X-linked intellectual disability, Atkin type Atkin-Flaitz syndrome is characterized by moderate to severe intellectual deficit, short stature, macrocephaly, and characteristic facies. It has been described in 11 males and three females from three successive generations of the same family. The males also presented with postpubertal macroorchidism. Transmission is X-linked. multiple congenital anomalies/dysmorphic syndrome-intellectual disability X-linked syndromic intellectual disability