هیپرپرولینمی تیپ I
Sign in to saveHyperprolinemia is a condition which occurs when the amino acid proline is not broken down properly by the enzymes proline oxidase or pyrroline-5-carboxylate dehydrogenase, causing a buildup of proline in the body.
In the Vinony graph
Vinony's link graph records 84 inbound references to هیپرپرولینمی تیپ I, and connects out to 1-pyrroline-5-carboxylate dehydrogenase, amino acid and public domain.
It sits within the topics Amino acid metabolism disorders, Autosomal recessive disorders and Disorders causing seizures.
Vinony links it to 5 Wikipedia language editions.
Research
209 papers- [Hyperprolinemia].Ryoikibetsu shokogun shirizu · 2001
- Psychiatric phenotypes associated with hyperprolinemia: A systematic review.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2021
- [Hyperprolinemia type Ⅰ caused by PRODH gene variation: 2 cases report and literature review].Zhonghua er ke za zhi = Chinese journal of pediatrics · 2023
- [Hyperprolinemia type II].Ryoikibetsu shokogun shirizu · 1998
- [Hyperprolinemia].Ryoikibetsu shokogun shirizu · 2000
via PubMed
Wikidata facts
Show 3 more facts
- exact match
- identifiers.org/doid/DOID:0080541
- on focus list of Wikimedia project
- WikiProject Medicine
- health specialty
- medical genetics
via Wikidata · CC0
Connections
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amino acid
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