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- Be374a64e4f3239f3c94e6f55fbab2f33 NCIT_P378 "NCI" @default.
- Be374a64e4f3239f3c94e6f55fbab2f33 type Axiom @default.
- Be374a64e4f3239f3c94e6f55fbab2f33 annotatedProperty IAO_0000115 @default.
- Be374a64e4f3239f3c94e6f55fbab2f33 annotatedSource NCIT_C35710 @default.
- Be374a64e4f3239f3c94e6f55fbab2f33 annotatedTarget "An autosomal recessive condition caused by mutation(s) in the AAAS gene encoding the protein ALADIN, and characterized by primary adrenal insufficiency, esophageal dysmotility, and absence of tear production." @default.