Rdh5

Cone dysfunction syndrome

Alternative names

Mode of inheritance

Visual acuity

Complete achromatopsia

Rod monochromatism

Autosomal recessive

6/36-6/60

Incomplete achromatopsia Blue cone monochromatism

Typical achromatopsia

Atypical achromatopsia X-linked atypical achromatopsia

X-linked incomplete achromatopsia

Autosomal recessive

X-linked

6/24-6/36 6/24-6/36

Oligocone trichromacy

Oligocone syndrome

Autosomal recessive

6/12-6/24

X-linked cone dysfunction syndrome with dichromacy and myopia

Bornholm eye disease

X-linked

6/12-6/36

LCR Locus control region

Refractive

Nystag

Colour

Fundi

Mutated gene(s)

error

mus

vision

Was this article helpful?

0 0

Post a comment