Search on: KERATODERMA, PALMOPLANTAR, EPIDERMOLYTIC 
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Descriptor English:   Keratoderma, Palmoplantar, Epidermolytic 
Descriptor Spanish:   Queratodermia Palmoplantar Epidermolítica 
Descriptor Portuguese:   Ceratodermia Palmar e Plantar Epidermolítica 
Tree Number:   C16.320.850.475.440.500
C17.800.428.435.440.500
C17.800.827.475.440.500
Definition English:   An autosomal dominant hereditary skin disease characterized by epidermolytic hyperkeratosis that is strictly confined to the palms and soles. It has been associated with mutations in the gene that codes for KERATIN-9. 
History Note English:   2007 
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:   52146 
Unique Identifier:   D053546 

Occurrence in VHL:
 

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