stromal antigen 2
OMIM: 300826,
ClinGen,
DECIPHER
| Panel | Reviews | Mode of inheritance | Details | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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STAG2 in Holoprosencephaly and septo-optic dysplasia
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2 reviews | Other |
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Phenotypes
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STAG2 in Mendeliome
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2 reviews | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) |
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Phenotypes
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STAG2 in Intellectual disability syndromic and non-syndromic
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1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) |
Sources
Phenotypes
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STAG2 in Clefting disorders
Level 3: Dysmorphic disorders
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1 review | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) |
Sources
Phenotypes
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STAG2 in Fetal anomalies
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2 reviews | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) |
Sources
Phenotypes
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