Hyperprolinemia is when there isan excess of a particular protein building block (amino acid), called proline, in the blood. This condition generally occurs when proline is not broken down properly by the body. There are two inherited forms:hyperprolinemia type1 and hyperprolinemia type 2. People with hyperprolinemia type I often do not show any symptoms, although they have proline levels in their blood between 3 and 10 times the normal level. Less commonly, affected individuals can experience seizures, intellectual disability, or other neurological or psychiatric problems. Hyperprolinemia is caused by mutations in the PRODH gene and is inherited in an autosomal recessive pattern. [ GARD:0002847 ]

This is just here as a test because I lose it

Term information

database cross reference
  • DOID:0080541 (MONDO:equivalentTo)
  • UMLS:C0268528 (MONDO:equivalentTo)
  • ICD9:270.8 (MONDO:relatedTo)
  • SCTID:59655002 (MONDO:equivalentTo)
Subsets

rare, nord_rare

exactMatch

http://purl.obolibrary.org/obo/DOID_0080541

http://identifiers.org/snomedct/59655002

http://linkedlifedata.com/resource/umls/id/C0268528

has related synonym

hyperprolinemia type 1

proline hydrogenase deficiency

proline oxidase deficiency

id

MONDO:0023419

seeAlso

https://rarediseases.info.nih.gov/diseases/2847/hyperprolinemia

Term relations