. . "Singleton Merten syndrome is an autosomal dominant genetic disorder with variable expression with an onset of symptoms during childhood."@en . "182250"^^ . . . . . "Singleton Merten syndrome"@en . . . "Q78.8"@en . "182250"^^ . . . . . . . . . . . . . "Singleton Merten syndrome is inherited in an autosomal dominant manner."@en . . . . . . . . . . . . . . . "1084540565"^^ . . . "3844"^^ . . . . . "Singleton Merten syndrome"@en . . . . . . . . . . . . . . . . . "85191"^^ . . . . . . . . . . . . . . "Singleton-Merten dysplasia"@en . . . . . . . "85191" . . . . . "Singleton Merten syndrome"@en . . "Q78.8" . "25193647"^^ . . "Singleton Merten syndrome is an autosomal dominant genetic disorder with variable expression with an onset of symptoms during childhood."@en . . . . . . . .