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Rare syndromic craniosynostosis or isolated multisuture synostosis v1.72 TGFBR1 Eleanor Williams Added phenotypes Loeys-Dietz syndrome 1 609192 for gene: TGFBR1
Rare syndromic craniosynostosis or isolated multisuture synostosis v1.47 TGFBR1 Tracy Lester reviewed gene: TGFBR1: Rating: GREEN; Mode of pathogenicity: Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments; Publications: 15731757; Phenotypes: Loeys-Dietz syndrome 1 - 609192; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Rare syndromic craniosynostosis or isolated multisuture synostosis v1.46 TGFBR1 Eleanor Williams reviewed gene: TGFBR1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Rare syndromic craniosynostosis or isolated multisuture synostosis v1.45 TGFBR1 Eleanor Williams Source NHS GMS was added to TGFBR1.
Rating Changed from Green List (high evidence) to Green List (high evidence)