Activity
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| Severe microcephaly v7.5 | MIR17HG | Arina Puzriakova Entity copied from Intellectual disability v8.19 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Severe microcephaly v7.5 | MIR17HG |
Arina Puzriakova gene: MIR17HG was added gene: MIR17HG was added to Severe microcephaly. Sources: Expert Review,Expert Review Amber deletions, watchlist, locus-type-rna-long-non-coding tags were added to gene: MIR17HG. Mode of inheritance for gene: MIR17HG was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: MIR17HG were set to 21892160; 19344873; 25391829; 26360630 Phenotypes for gene: MIR17HG were set to Feingold syndrome 2, 614326; FS2; Brachydactyly with short stature and microcephaly; Intellectual disability Penetrance for gene: MIR17HG were set to Complete |
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