O-linked N-acetylglucosamine (GlcNAc) transferase
OMIM: 300255, Gene2Phenotype
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OGT in Congenital Disorders of Glycosylation
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1 review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
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Phenotypes
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OGT in Mendeliome
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1 review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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OGT in Genetic Epilepsy
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3 reviews | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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OGT in Intellectual disability syndromic and non-syndromic
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1 review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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