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| Hypogonadotropic hypogonadism v1.0 | PRDM13 | Gene migrated from ENSG00000112238 to ENSG00000112238 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hypogonadotropic hypogonadism v0.68 | Chirag Patel Copied gene PRDM13 from panel Differences of Sex Development | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hypogonadotropic hypogonadism v0.68 | PRDM13 |
Chirag Patel gene: PRDM13 was added gene: PRDM13 was added to Hypogonadotropic hypogonadism. Sources: Expert Review Amber,Literature founder tags were added to gene: PRDM13. Mode of inheritance for gene: PRDM13 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: PRDM13 were set to 34730112 Phenotypes for gene: PRDM13 were set to Cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism, MIM# 619761 |
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