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- B93da26e4e77d102c6bdfdfa043d1d2ce NCIT_P378 "NICHD" @default.
- B93da26e4e77d102c6bdfdfa043d1d2ce type Axiom @default.
- B93da26e4e77d102c6bdfdfa043d1d2ce annotatedProperty NCIT_P325 @default.
- B93da26e4e77d102c6bdfdfa043d1d2ce annotatedSource NCIT_C26900 @default.
- B93da26e4e77d102c6bdfdfa043d1d2ce annotatedTarget "A condition caused by absence of part or all of the second sex chromosome in an individual with female phenotype, resulting in a variable constellation of physical and functional anomalies. Characteristic clinical features may include, but are not limited to, short stature, premature ovarian failure, cardiac anomalies, renal anomalies, skeletal variations, and hearing impairment." @default.