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| Skeletal dysplasia v1.0 | HOXD13_SPD1_GCG | STR HOXD13_SPD1_GCG: gene migrated from ENSG00000128714 to ENSG00000128714 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v0.372 | Bryony Thompson Copied STR HOXD13_SPD1_GCG from panel Repeat Disorders | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v0.372 | HOXD13_SPD1_GCG |
Bryony Thompson STR: HOXD13_SPD1_GCG was added STR: HOXD13_SPD1_GCG was added to Skeletal dysplasia. Sources: Expert Review Green,Expert list paediatric-onset tags were added to STR: HOXD13_SPD1_GCG. Mode of inheritance for STR: HOXD13_SPD1_GCG was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for STR: HOXD13_SPD1_GCG were set to 8817328; 33811808; 33533119 Phenotypes for STR: HOXD13_SPD1_GCG were set to Synpolydactyly 1 MIM#186000 |
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