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- Bb8340a5ee7ae77ab55e5538ef218bf7c NCIT_P378 "NCI" @default.
- Bb8340a5ee7ae77ab55e5538ef218bf7c type Axiom @default.
- Bb8340a5ee7ae77ab55e5538ef218bf7c annotatedProperty IAO_0000115 @default.
- Bb8340a5ee7ae77ab55e5538ef218bf7c annotatedSource NCIT_C35710 @default.
- Bb8340a5ee7ae77ab55e5538ef218bf7c 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.