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| Hereditary Spastic Paraplegia v2.0 | BICD2 | Gene migrated from ENSG00000185963 to ENSG00000185963 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Spastic Paraplegia v1.107 | Bryony Thompson Copied gene BICD2 from panel Hereditary Spastic Paraplegia - adult onset | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hereditary Spastic Paraplegia v1.107 | BICD2 |
Bryony Thompson gene: BICD2 was added gene: BICD2 was added to Hereditary Spastic Paraplegia. Sources: Expert Review Amber,Expert list Mode of inheritance for gene: BICD2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: BICD2 were set to 23664120; 25497877; 24482476 Phenotypes for gene: BICD2 were set to Spinal muscular atrophy, lower extremity-predominant, 2A, autosomal dominant, MIM#615290; Spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant, MIM#618291 |
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