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| Intellectual disability syndromic and non-syndromic v2.155 | CHD9 | Zornitza Stark Marked gene: CHD9 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.155 | CHD9 | Zornitza Stark Gene: chd9 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.155 | Zornitza Stark Copied gene CHD9 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Intellectual disability syndromic and non-syndromic v2.155 | CHD9 |
Zornitza Stark gene: CHD9 was added gene: CHD9 was added to Intellectual disability syndromic and non-syndromic. Sources: Expert Review Red,Literature Mode of inheritance for gene: CHD9 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: CHD9 were set to 42640505; 35183220 Phenotypes for gene: CHD9 were set to Neurodevelopmental disorder, MONDO:0700092, CHD9-related |
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