disease has feature Amblyopia amblyopia color vision disorder retinal disorder achromatopsia https://www.malacards.org/card/achromatopsia SCTID:102450007 DOID:13911 Orphanet:49382 Rod monochromatism Pingelapese blindness NCIT:C84528 ICD9:368.54 Rod monochromacy 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. ICD10CM:H53.51 Editor note: we include incomplete forms here, such as BCM ACHM total color blindness complete or incomplete colour blindness MedDRA:10000454 complete or incomplete color blindness UMLS:C0152200 total colour blindness MONDO:0018852 GARD:0015015 MEDGEN:57751 achromatopsia