Preferred Label : McDonough syndrome;
ICD-11 definition : McDonough syndrome belongs to the group of multiple congenital anomalies/mental retardation
(MCA/MR) syndromes and is characterised by intellectual deficit, distinctive facies
(upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism,
and a congenital heart defect.;
Origin ID : 1349711155;
Currated CISMeF NLP mapping
McDonough syndrome belongs to the group of multiple congenital anomalies/mental retardation
(MCA/MR) syndromes and is characterised by intellectual deficit, distinctive facies
(upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism,
and a congenital heart defect.
