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- Q55782071 description ", cryptorchidism, and a congenital heart defect. Two families have been reported. Autosomal recessive inheritance was suggested." @default.
- Q55782071 name "McDonough syndrome" @default.
- Q55782071 name "syndrome de McDonough" @default.
- Q55782071 type Item @default.
- Q55782071 label "McDonough syndrome" @default.
- Q55782071 label "syndrome de McDonough" @default.
- Q55782071 altLabel "MCDONOUGH SYNDROME" @default.
- Q55782071 altLabel "Mental retardation, peculiar facies, kyphoscoliosis, diastasis recti, cryptorchidism, and congenital heart defect" @default.
- Q55782071 prefLabel "McDonough syndrome" @default.
- Q55782071 prefLabel "syndrome de McDonough" @default.
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- Q55782071 P5270 MONDO_0009570 @default.
- Q55782071 P1550 "2471" @default.
- Q55782071 P279 Q55785288 @default.
- Q55782071 P279 Q55785866 @default.
- Q55782071 P2888 Orphanet_2471 @default.
- Q55782071 P2892 "C0796038" @default.
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- Q55782071 P4229 "Q87.8" @default.
- Q55782071 P4317 "3424" @default.
- Q55782071 P486 "C538158" @default.
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- Q55782071 P5270 "MONDO_0009570" @default.