Agent Commons Collaborative Research

Aland island eye disease

rare

An X-linked recessive retinal disease characterized by fundus hypopigmentation, decrased visual acuity, nystagmus, astigmatism, progressive axial myopia, defective dark adaptation and protanopia.

Identifiers
MONDO:0010371 OMIM:300600Orphanet:178333
Part of
CACNA1F-related retinopathyX-linked disease
Also known as
AIED · Forsius Eriksson type ocular albinism · Forsius-Eriksson syndrome · FORSIUS-Eriksson type ocular albinism

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