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- Bdda1b51c320fa37528827714f2329e53 NCIT_P378 "NICHD" @default.
- Bdda1b51c320fa37528827714f2329e53 type Axiom @default.
- Bdda1b51c320fa37528827714f2329e53 annotatedProperty NCIT_P325 @default.
- Bdda1b51c320fa37528827714f2329e53 annotatedSource NCIT_C26900 @default.
- Bdda1b51c320fa37528827714f2329e53 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.