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ERYTHROKERATODERMIA VARIABILIS
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DeCS
Descriptor
English
:
Erythrokeratodermia Variabilis
Descriptor
Spanish
:
Eritroqueratodermia Variable
Descriptor
Portuguese
:
Eritroceratodermia Variável
Synonyms
English
:
Erythrokeratodermia Figurata Variabilis
Greither Disease
Mendes De Costa Syndrome
Tree Number:
C16.320.850.337
C17.800.229.606
C17.800.428.304
C17.800.827.337
Definition
English
:
An autosomal dominant skin
disease
characterized by transient and variable noninflammatory
ERYTHEMA
and hyperkeratosis. It has been associated with mutations in the genes that code for
CONNEXINS
.
Erythrokeratodermia variabilis
inherited in an autosomal recessive fashion has also been reported. Affected individuals often develop PALMOPLANTAR KERATODERMA.
See Related
English
:
Connexins
Keratoderma, Palmoplantar
History Note
English
:
2010
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:
53558
Unique Identifier:
D056266
Occurrence in VHL
:
Similar:
DeCS
CID-10
SciELO
LILACS
LIS