has material basis in germline mutation in FGD1 X-linked disease FG syndrome Aarskog-Scott syndrome, X-linked https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/aarskog_scott_syndrome SCTID:14921002 OMIM:305400 FGD MRXS16, included Aarskog-Scott syndrome AAS MedDRA:10067148 FGDY MEDGEN:61234 MONDO:0010589 Aarskog-like syndrome mental retardation, X-linked syndromic 16, X-linked recessive DOID:6683 ICD9:759.89 faciogenital dysplasia Aarskog disease Aarskog syndrome mental retardation, X-linked, syndromic 16, included Aarskog Scott syndrome Aarskog-Scott syndrome, X-linked recessive UMLS:C0175701 Scott Aarskog syndrome Aarskog-Scott syndrome, X-linked faciodigitogenital syndrome MESH:C535331 NCIT:C129720 mental retardation, X-linked, syndromic 16 GARD:0024738 faciodigitogenital syndrome, recessive Aarskog-Scott syndrome (AAS) is a rare developmental disorder characterized by facial, limbs and genital features, and a disproportionate acromelic short stature. facio-digito-genital dysplasia Aarskog syndrome, X-linked faciogenital dysplasia with attention Deficit-hyperactivity disorder multiple congenital anomalies/dysmorphic syndrome-intellectual disability multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome X-linked syndromic intellectual disability faciodigitogenital syndrome