Palmoplantar keratoderma
Palmoplantar keratodermas are a heterogeneous group of disorders characterized by abnormal thickening of the palms and soles. Autosomal recessive and dominant, X-linked, and acquired forms have all been described.
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Acquired aquagenic palmoplantar keratodermaAcquired aquagenic syringeal acrokeratodermaAcquired keratosis (keratoderma) palmaris et plantarisAcrokeratoelastoidosis lichenoidesAquagenic KeratodermaAquagenic keratodermaAquagenic syringeal acrokeratodermaAquagenic wrinkling of the palmsAutosomal-dominant hereditary punctate keratoderma associated with malignancyBrünauer-Fuhs-Siemens PPKBrünauer-Fuhs-Siemens type of palmoplantar keratodermaBrünauer–Fuhs–Siemens PPKBrünauer–Fuhs–Siemens type of palmoplantar keratodermaBuschke-Fischer-Brauer diseaseBuschke–Fischer–Brauer diseaseCarvajal syndromeCharcot-Marie-Tooth disease with palmoplantar keratoderma and nail dystrophyCharcot–Marie–Tooth disease with palmoplantar keratoderma and nail dystrophyDavis Colley diseaseDegenerative collagenous plaques of the handDiffuse epidermolytic PPKDiffuse epidermolytic palmoplantar keratodermaDiffuse nonepidermolytic PPKDiffuse nonepidermolytic palmoplantar keratodermaDiffuse orthohyperkeratotic keratodermaDiffuse palmoplantar keratodermaFocal acral hyperkeratosisFocal epidermolytic PPKFocal epidermolytic palmoplantar keratodermaFocal non-epidermolytic PPKFocal non-epidermolytic palmoplantar keratodermaFocal palmoplantar keratodermaFocal palmoplantar keratoderma with oral mucosal hyperkeratosisGreither keratodermaGreither palmoplantar keratodermaGreither syndromeGreither typeHereditary painful callositiesHereditary painful callosity syndromeHereditary palmoplantar keratoderma
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Acquired aquagenic palmoplantar keratodermaAcquired aquagenic syringeal acrokeratodermaAcquired keratosis (keratoderma) palmaris et plantarisAcral keratodermaAcrokeratoelastoidosisAcrokeratoelastoidosis lichenoidesAinhumAquagenic KeratodermaAquagenic keratodermaAquagenic syringeal acrokeratodermaAquagenic wrinkling of the palmsArrhythmogenic cardiomyopathyArthur ThostAutosomal-dominant hereditary punctate keratoderma associated with malignancyBart–Pumphrey syndromeBruno ReversadeBrünauer-Fuhs-Siemens PPKBrünauer-Fuhs-Siemens type of palmoplantar keratodermaBrünauer–Fuhs–Siemens PPKBrünauer–Fuhs–Siemens type of palmoplantar keratodermaBuschke-Fischer-Brauer diseaseBuschke–Fischer–Brauer diseaseCamisa diseaseCarvajalCarvajal syndromeCerebral dysgenesis–neuropathy–ichthyosis–keratoderma syndromeCharcot-Marie-Tooth disease with palmoplantar keratoderma and nail dystrophyCharcot–Marie–Tooth disease with palmoplantar keratoderma and nail dystrophyChemotherapy-induced acral erythemaClouston's hidrotic ectodermal dysplasiaConnexinCorneodermatoosseous syndromeCowden syndromeDavis Colley diseaseDegenerative collagenous plaques of the handDermatopathia pigmentosa reticularisDesmocollinDesmoplakinDesmosomeDiffuse epidermolytic PPK
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Palmoplantar keratoderma
Palmoplantar keratodermas are a heterogeneous group of disorders characterized by abnormal thickening of the palms and soles. Autosomal recessive and dominant, X-linked, and acquired forms have all been described.
has abstract
Ceratodermia palmoplantar é um ...... s, relacionadas com o sexo e .
@pt
Eine hereditäre Palmoplantarke ...... rnungsstörung (Hyperkeratose).
@de
La cheratodermia di Sybert è u ...... missione autosomica dominante.
@it
Las queratodermias palmoplanta ...... gados al sexo y adquiridas.
@es
Palmoplantar keratodermas are ...... forms have all been described.
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DiseasesDB
eMedicine subject
derm
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eMedicine topic
589
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ICD10
ICD9
MeSH ID
OMIM id
Wikipage page ID
page length (characters) of wiki page
Wikipage revision ID
1,010,113,445
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caption
Patient with severe keratosis.
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DiseasesDB
eMedicineSubj
derm
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eMedicineTopic
ICD
@en
, Q82.8
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,
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-
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L85.1
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L85.2
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MeshID
D007645
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name
Palmoplantar keratoderma
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OMIM
SNOMED CT
706,885,006
wikiPageUsesTemplate
wordnet_type
hypernym
comment
Ceratodermia palmoplantar é um ...... s, relacionadas com o sexo e .
@pt
Eine hereditäre Palmoplantarke ...... rnungsstörung (Hyperkeratose).
@de
La cheratodermia di Sybert è u ...... missione autosomica dominante.
@it
Las queratodermias palmoplanta ...... gados al sexo y adquiridas.
@es
Palmoplantar keratodermas are ...... forms have all been described.
@en
label
Ceratodermia palmoplantar
@pt
Cheratodermia di Sybert
@it
Hereditäre Palmoplantarkeratose
@de
Palmoplantar keratoderma
@en
Queratodermia palmoplantar
@es
sameAs
wasDerivedFrom
isPrimaryTopicOf
name
Palmoplantar keratoderma
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