solute carrier family 9 member A7
OMIM: 300368,
ClinGen,
DECIPHER
| Panel | Reviews | Mode of inheritance | Details | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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SLC9A7 in Congenital Disorders of Glycosylation
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1 review | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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SLC9A7 in Mendeliome
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2 reviews | X-LINKED: hemizygous mutation in males, biallelic mutations in females |
Sources
Phenotypes
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SLC9A7 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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