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| Growth failure in early childhood v0.61 | SPRED1 | Ivone Leong Classified gene: SPRED1 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Growth failure in early childhood v0.61 | SPRED1 | Ivone Leong Gene: spred1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Growth failure in early childhood v0.60 | SPRED1 | Ivone Leong changed review comment from: After clinical discussion it was decided to keep SPRED1 amber as the growth phenotype is not predominant.; to: After clinical discussion it was decided that SPRED1 is demoted to red status as the growth phenotype is not predominant and therefore not appropriate for this panel. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Growth failure in early childhood v0.60 | SPRED1 | Ivone Leong commented on gene: SPRED1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Growth failure in early childhood v0.27 | SPRED1 | Rebecca Foulger reviewed gene: SPRED1: Rating: AMBER; Mode of pathogenicity: ; Publications: 17704776, 19366998, 19443465, 21649642, 21548021; Phenotypes: Legius Syndrome, Neurofibromatosis-like syndrome; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Growth failure in early childhood v0.26 | SPRED1 |
Rebecca Foulger gene: SPRED1 was added gene: SPRED1 was added to Growth failure in early childhood. Sources: Expert Review Amber Mode of inheritance for gene: SPRED1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: SPRED1 were set to 19443465; 21548021; 21649642; 19366998; 17704776 Phenotypes for gene: SPRED1 were set to Legius Syndrome; Neurofibromatosis-like syndrome |
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