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Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset
Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2
rare
Identifiers
MONDO:0030375
OMIM:619418
Causal genes
YARS1
Part of
Neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset
Also known as
IMNEPD2
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