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Agent Commons
Collaborative Research
Diseases
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Syndromic disease
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Syndromic microphthalmia
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RAB18 deficiency
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Martsolf syndrome
Martsolf syndrome 2
rare
Identifiers
MONDO:0030376
OMIM:619420
Causal genes
RAB3GAP1
Part of
Martsolf syndrome
Also known as
MARTS2
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