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Phosphohydroxylysinuria(PHLU)

MedGen UID:
767258
Concept ID:
C3554344
Finding
Synonym: PHLU
 
Gene (location): PHYKPL (5q35.3)
 
HPO: HP:0031870
Monarch Initiative: MONDO:0014008
OMIM®: 615011

Definition

Phosphohydroxylysinuria (PHLU) is characterized by elevated phosphohydroxylysine in the urine. There is no clinical phenotype associated with this finding other than the urinary metabolites. This was confirmed by population genetic studies performed by Veiga-da-Cunha et al. (2013) (Hamosh, 2013). [from OMIM]

Clinical features

From HPO
Phosphohydroxylysinuria
MedGen UID:
767258
Concept ID:
C3554344
Finding
Phosphohydroxylysinuria (PHLU) is characterized by elevated phosphohydroxylysine in the urine. There is no clinical phenotype associated with this finding other than the urinary metabolites. This was confirmed by population genetic studies performed by Veiga-da-Cunha et al. (2013) (Hamosh, 2013).

Conditions with this feature

Phosphohydroxylysinuria
MedGen UID:
767258
Concept ID:
C3554344
Finding
Phosphohydroxylysinuria (PHLU) is characterized by elevated phosphohydroxylysine in the urine. There is no clinical phenotype associated with this finding other than the urinary metabolites. This was confirmed by population genetic studies performed by Veiga-da-Cunha et al. (2013) (Hamosh, 2013).

Recent clinical studies

Etiology

Veiga-da-Cunha M, Hadi F, Balligand T, Stroobant V, Van Schaftingen E
J Biol Chem 2012 Mar 2;287(10):7246-55. Epub 2012 Jan 12 doi: 10.1074/jbc.M111.323485. PMID: 22241472Free PMC Article

Clinical prediction guides

Dorland L, Duran M, de Bree PK, Smith GR, Horvath A, Tibosch AS, Wadman SK
Clin Chim Acta 1990 May;188(3):221-6. doi: 10.1016/0009-8981(90)90203-5. PMID: 2387074

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