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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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Familial glucocorticoid deficiency
Glucocorticoid deficiency 3
rare
Identifiers
MONDO:0012214
OMIM:609197
Part of
Familial glucocorticoid deficiency
Also known as
GCCD3 · glucocorticoid deficiency 2
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