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- Babbd0baf08baa96a22d5bd4a1e144b76 hasDbXref "Orphanet:49382" @default.
- Babbd0baf08baa96a22d5bd4a1e144b76 type Axiom @default.
- Babbd0baf08baa96a22d5bd4a1e144b76 annotatedProperty IAO_0000115 @default.
- Babbd0baf08baa96a22d5bd4a1e144b76 annotatedSource MONDO_0018852 @default.
- Babbd0baf08baa96a22d5bd4a1e144b76 annotatedTarget "Achromatopsia (ACHM) is a rare autosomal recessive retinal disorder characterized by color blindness, nystagmus, photophobia, and severely reduced visual acuity due to the absence or impairment of cone function." @default.