Disease #04552 (hydroxykynureninuria?, OMIM:236800)

Official abbreviation -
Name hydroxykynureninuria?
OMIM ID 236800
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene KYNU
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00303205 family PubMed: Christensen 2007 2-generation family, 2 affected brothers, unaffected heterozygous carrier parents M - Denmark - - - - - hydroxykynureninuria? massive urinary excretion of xanthurenic acid, 3-hydroxykynurenine and kynurenine KYNU KYNU 1 2 Johan den Dunnen
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