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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Inherited primary ovarian failure
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Perrault syndrome
Perrault syndrome 6
rare
Identifiers
MONDO:0033047
OMIM:617565
Causal genes
ERAL1
Part of
Perrault syndrome
Also known as
PRLTS6
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