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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Neurodevelopmental disorder
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Intellectual disability
Intellectual developmental disorder and retinitis pigmentosa; IDDRP
rare
Identifiers
MONDO:0032594
OMIM:618195
Causal genes
SCAPER
Part of
Mendelian neurodevelopmental disorder
Intellectual disability
Also known as
IDDRP
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