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| Hypogonadotropic hypogonadism v1.0 | TCF12 | Gene migrated from ENSG00000140262 to ENSG00000140262 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hypogonadotropic hypogonadism v0.47 | Chirag Patel Copied gene TCF12 from panel Differences of Sex Development | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hypogonadotropic hypogonadism v0.47 | TCF12 |
Chirag Patel gene: TCF12 was added gene: TCF12 was added to Hypogonadotropic hypogonadism. Sources: Expert Review Green,Literature Mode of inheritance for gene: TCF12 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal Publications for gene: TCF12 were set to 32620954 Phenotypes for gene: TCF12 were set to Hypogonadotropic hypogonadism 26 with or without anosmia, MIM# 619718; Kallmann syndrome |
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