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- B3599efd0c570455c9896a418c398f19c hasDbXref "Wikipedia:Hyper-IgM_syndrome_type_1" @default.
- B3599efd0c570455c9896a418c398f19c type Axiom @default.
- B3599efd0c570455c9896a418c398f19c annotatedProperty IAO_0000115 @default.
- B3599efd0c570455c9896a418c398f19c annotatedSource MONDO_0010626 @default.
- B3599efd0c570455c9896a418c398f19c annotatedTarget "The X-linked variant of the Hyper-IgM syndrome. The affected individuals are virtually always male, because males only have one X chromosome, received from their mothers. Their mothers are not symptomatic, even though they are carriers of the allele, because the trait is recessive. Male offspring of these women have a 50% chance of inheriting their mother's mutant allele." @default.