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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Inherited retinal dystrophy
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Hereditary macular dystrophy
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Patterned dystrophy of the retinal pigment epithelium
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Reticular dystrophy of the retinal pigment epithelium
RCBTB1-related retinopathy
rare
Identifiers
MONDO:0014955
OMIM:617175
Causal genes
RCBTB1
Part of
Reticular dystrophy of the retinal pigment epithelium
Also known as
RDEOA · retinal dystrophy with or without extraocular anomalies
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