phosphoglycerate kinase 1
OMIM: 311800, Gene2Phenotype
Panel | Reviews | Mode of inheritance | Details | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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PGK1 in Early-onset Parkinson disease
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
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Phenotypes
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PGK1 in Glycogen Storage Diseases
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
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Phenotypes
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PGK1 in Mendeliome
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
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Phenotypes
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PGK1 in Intellectual disability syndromic and non-syndromic
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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PGK1 in Rhabdomyolysis and Metabolic Myopathy
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
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Phenotypes
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PGK1 in Mackenzie's Mission_Reproductive Carrier Screening
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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PGK1 in Red cell disorders
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
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Phenotypes
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PGK1 in Prepair 1000+
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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PGK1 in Prepair 500+
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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