Search on: PORPHYRIA CUTANEA TARDA 
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Descriptor English:   Porphyria Cutanea Tarda 
Descriptor Spanish:   Porfiria Cutánea Tardía 
Descriptor Portuguese:   Porfiria Cutânea Tardia 
Tree Number:   C06.552.830.100
C16.320.850.742.250
C17.800.827.742.250
C18.452.811.400.250
Definition English:   An autosomal dominant or acquired porphyria due to a deficiency of UROPORPHYRINOGEN DECARBOXYLASE in the LIVER. It is characterized by photosensitivity and cutaneous lesions with little or no neurologic symptoms. Type I is the acquired form and is strongly associated with liver diseases and hepatic toxicities caused by alcohol or estrogenic steroids. Type II is the familial form. 
History Note English:   95; was PORPHYRIA, CUTANEA TARDA 1993-94 
Allowable Qualifiers English:  
BL blood CF cerebrospinal fluid
CI chemically induced CL classification
CO complications CN congenital
DI diagnosis DG diagnostic imaging
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
RT radiotherapy RH rehabilitation
SU surgery TH therapy
UR urine VE veterinary
VI virology  
Record Number:   30608 
Unique Identifier:   D017119 

Occurrence in VHL:
 

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