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| Growth failure v2.0 | ERBB2 | Gene migrated from ENSG00000141736 to ENSG00000141736 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Growth failure v1.109 | Sarah Milton Copied gene ERBB2 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Growth failure v1.109 | ERBB2 |
Sarah Milton gene: ERBB2 was added gene: ERBB2 was added to Growth failure. Sources: Expert Review Amber,Victorian Clinical Genetics Services Mode of inheritance for gene: ERBB2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: ERBB2 were set to 40329538; 33720042 Phenotypes for gene: ERBB2 were set to Congenital heart disease - left ventricular outflow tract obstruction defects; MONDO:0005453; Hirschsprung disease (HSCR, aganglionic megacolon, MIM#142623) |
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