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| Vitamin metabolism disorders v2.0 | ALPL | Gene migrated from ENSG00000162551 to ENSG00000162551 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Vitamin metabolism disorders v1.2 | ALPL |
Bryony Thompson gene: ALPL was added gene: ALPL was added to Vitamin metabolism disorders. Sources: Expert review Green Mode of inheritance for gene: ALPL was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: ALPL were set to 3174660, 1409720 Phenotypes for gene: ALPL were set to disorder of bone metabolism; Hypophosphatasia; Disorders of pyridoxine metabolism |
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