steroid sulfatase
OMIM: 300747, Gene2Phenotype
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STS in Corneal Dystrophy
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
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Phenotypes
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STS in Ichthyosis
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
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Phenotypes
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STS in Mendeliome
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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STS in Palmoplantar Keratoderma and Erythrokeratoderma
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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STS in Additional findings_Paediatric
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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STS in Miscellaneous Metabolic 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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STS in BabyScreen+ newborn screening
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review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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