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| Lipodystrophy - childhood onset v0.17 | ADRA2A | Ivone Leong Marked gene: ADRA2A as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Lipodystrophy - childhood onset v0.17 | ADRA2A | Ivone Leong Gene: adra2a has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Lipodystrophy - childhood onset v0.14 | ADRA2A | Ivone Leong Marked gene: ADRA2A as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Lipodystrophy - childhood onset v0.14 | ADRA2A | Ivone Leong Added comment: Comment when marking as ready: ARDRA2A was included in this panel as a red gene as suggested by Keven Colclough (Royal Devon & Exeter Hospital). Familial partial lipodystrophy is not confirmed to be associated with ADRA2A in OMIM or Gene2Phenotype. There is only one variant reported (PMID: 27376152). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Lipodystrophy - childhood onset v0.14 | ADRA2A | Ivone Leong Gene: adra2a has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Lipodystrophy - childhood onset v0.10 | ADRA2A |
Ivone Leong gene: ADRA2A was added gene: ADRA2A was added to Lipodystrophy - childhood onset. Sources: Expert list,Literature Mode of inheritance for gene: ADRA2A was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: ADRA2A were set to 27376152 Phenotypes for gene: ADRA2A were set to No OMIM number; familial partial lipodystrophy |
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