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.

Synonyms: Rod monochromatism Complete or incomplete color blindness Rod monochromacy ACHM Pingelapese blindness Total color blindness

This is just here as a test because I lose it

Term information

database cross reference
hasDbXref

UMLS:C0152200

OMIM:216900

OMIM:610024

OMIM:613856

OMIM:262300

OMIM:613093

MedDRA:10000454

OMIM:616517

ICD-10:H53.5

notation

ORPHA:49382