hyperprolinemia type 2 (Q66084704)
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hyperprolinemia that has material basis in homozygous or compound heterozygous mutation in the pyrroline-5-carboxylate dehydrogenase gene on chromosome 1p36
- hyperprolinemia type II
- HYRPRO2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hyperprolinemia type 2 |
hyperprolinemia that has material basis in homozygous or compound heterozygous mutation in the pyrroline-5-carboxylate dehydrogenase gene on chromosome 1p36 |
|
Statements
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Identifiers
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1 reference