hyperprolinemia type 1 (Q66084703)
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hyperprolinemia that has material basis in homozygous or compound heterozygous mutation in the proline dehydrogenase gene on chromosome 22q11
- hyperprolinemia type I
- HYRPRO1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | hyperprolinemia type 1 |
hyperprolinemia that has material basis in homozygous or compound heterozygous mutation in the proline dehydrogenase gene on chromosome 22q11 |
|
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