Orphanet classification of rare genetic diseases
- Rare genetic disease
ORPHA:98053 -
ORPHA:71859 -
ORPHA:183757
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- Rare genetic disease
ORPHA:98053 -
ORPHA:68367 -
ORPHA:79161 -
ORPHA:79177 -
ORPHA:3008 -
Pyruvate carboxylase deficiency, benign type
ORPHA:353320
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