Search on: ALKAPTONURIA 
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Descriptor English:   Alkaptonuria 
Descriptor Spanish:   Alcaptonuria 
Descriptor Portuguese:   Alcaptonúria 
Tree Number:   C16.320.565.100.187
C18.452.648.100.187
Definition English:   An inborn error of amino acid metabolism resulting from a defect in the enzyme HOMOGENTISATE 1,2-DIOXYGENASE, an enzyme involved in the breakdown of PHENYLALANINE and TYROSINE. It is characterized by accumulation of HOMOGENTISIC ACID in the urine, OCHRONOSIS in various tissues, and ARTHRITIS. 
Allowable Qualifiers English:  
blood cerebrospinal fluid
chemically induced classification
complications diet therapy
diagnosis drug therapy
economics ethnology
embryology enzymology
epidemiology etiology
genetics history
immunology metabolism
microbiology mortality
nursing pathology
prevention & control physiopathology
parasitology psychology
radiography rehabilitation
radionuclide imaging radiotherapy
surgery therapy
urine ultrasonography
veterinary virology
Record Number:   476 
Unique Identifier:   D000474 

Occurrence in VHL:
 

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