Any syndromic congenital malformation characterized by reduced fetal growth, a short-spine, a long and narrow face, cardiac defects and heterotopy of the spiral colon that occurs in newborn cattle due to a mutation in the MAP2K2 gene.
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Phelan-McDermid syndrome, non-human animal
MONDO:1010006
atrial septal defect, non-human animal
MONDO:1010009
patent ductus arteriosus, non-human animal
MONDO:1010017
supravalvular aortic stenosis, non-human animal
MONDO:1010020
tetralogy of fallot, non-human animal
MONDO:1010021
ventricular septal defect, non-human animal
MONDO:1010022