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. 
See Related English:   Homogentisate 1,2-Dioxygenase
 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications DI diagnosis
DH diet therapy DT drug therapy
EC economics EM embryology
EN enzymology EP epidemiology
EH ethnology ET etiology
GE genetics HI history
IM immunology ME metabolism
MI microbiology MO mortality
NU nursing PS parasitology
PA pathology PP physiopathology
PC prevention & control PX psychology
RA radiography RI radionuclide imaging
RT radiotherapy RH rehabilitation
SU surgery TH therapy
US ultrasonography UR urine
VE veterinary VI virology
Record Number:   476 
Unique Identifier:   D000474 

Occurrence in VHL:
 

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