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Ontology Browser
Term:
Parent Terms Term With Siblings Child Terms
Genetic Skin Diseases +     
keratosis +     
acquired hyperkeratosis 
acrokeratosis verruciformis  
actinic keratosis +   
Actinic Prurigo  
adermatoglyphia  
Albinism +   
Annular Erythema 
arterial tortuosity syndrome  
atopic dermatitis +   
Atrophia Maculosa Varioliformis Cutis, Familial 
Autoinflammation with Arthritis and Dyskeratosis  
autosomal recessive congenital ichthyosis +   
Basaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant 
Bloch-Sulzberger syndrome +   
bullous congenital ichthyosiform erythroderma  
Buschke-Ollendorff syndrome  
Callosities +  
cherubism +   
cholesteatoma +   
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Curly Hair-Acral Keratoderma-Caries Syndrome 
Cutaneous Bullous Amyloidosis 
cutaneous porphyria  
cutis laxa +   
Defect in Hyaluronan Metabolism 
Dowling-Degos disease +   
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
epidermolysis bullosa +   
epidermolytic hyperkeratosis +   
erythrokeratodermia variabilis +   
Familial Reactive Perforating Collagenosis 
geroderma osteodysplasticum  
Hailey-Hailey disease  
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
hereditary papulotranslucent acrokeratoderma 
Hereditary Sclerosing Poikiloderma +   
Histiocytic Dermatoarthritis 
hyaline fibromatosis syndrome  
Hyperkeratosis Lenticularis Perstans 
ichthyosis +   
ichthyosis vulgaris +   
Isolated Osteopoikilosis 
Johnston Aarons Schelley Syndrome 
Juvenile Spring Eruption of Ears 
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
lipoid proteinosis  
monilethrix +   
Muir-Torre syndrome  
Multiple Eruptive Milia 
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
Oculotrichodysplasia 
orofaciodigital syndrome IX  
palmoplantar keratosis +   
A keratosis characterized by abnormal thickening of the palms and the soles. (DO)
Parakeratosis  
Parana Hard Skin Syndrome 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
peeling skin syndrome +   
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
Perioral Pigmented Follicular Atrophoderma with Milia and Epidermoid Cysts 
PLACK syndrome  
plasminogen deficiency type I  
poikiloderma with neutropenia  
porokeratosis +   
primary cutaneous amyloidosis +   
progressive osseous heteroplasia  
Progressive Vitiligo with Mental Retardation and Urethral Duplication 
prolidase deficiency  
pseudoxanthoma elasticum +   
Rothmund-Thomson syndrome +   
Sclerotylosis  
seborrheic keratosis +   
Sjogren-Larsson syndrome +   
spinocerebellar ataxia type 34  
stiff skin syndrome  
Storm Syndrome 
Trichostasis Spinulosa 
trichothiodystrophy +   
Urban Schosser Spohn Syndrome  
Vohwinkel Syndrome, Variant Form  
white sponge nevus +   
X-linked ichthyosis +   
X-linked reticulate pigmentary disorder  
xeroderma pigmentosum +   
 Alopecia Congenita Keratosis Palmoplantaris +   
 Bart-Pumphrey syndrome  
 Basaran Yilmaz Syndrome  
 Cancer, Alopecia, Pigment Dyscrasia, Onychodystrophy, and Keratoderma  
 CEDNIK syndrome  
 Cole Disease  
 Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
 Corneodermatoosseous Syndrome 
 Diffuse Palmoplantar Keratoderma +   
 Fitzsimmons-McLachlan-Gilbert syndrome 
 focal palmoplantar and gingival keratosis 
 Hyperkeratosis-Hyperpigmentation Syndrome 
 Hypotrichosis-Osteolysis-Periodontitis-Palmoplantar Keratoderma Syndrome 
 inflammatory poikiloderma with hair abnormalities and acral keratoses  
 Judge Misch Wright Syndrome 
 Keratoderma Palmoplantaris Transgrediens  
 Keratoderma-Ichthyosis-Deafness Syndrome, Autosomal Recessive  
 Keratosis Palmaris et Plantaris with Clinodactyly 
 keratosis palmoplantaris striata +   
 mal de Meleda  
 mutilating palmoplantar keratoderma with periorificial keratotic plaques +   
 Naegeli-Franceschetti-Jadassohn syndrome  
 nonepidermolytic palmoplantar keratoderma +   
 Palmoplantar Hyperkeratosis and True Hermaphroditism  
 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and Sex Reversal  
 Palmoplantar Keratoderma, Norrbotten Recessive Type  
 Palmoplantar Keratoderma, Spastic Paralysis 
 palmoplantar keratoderma-deafness syndrome  
 palmoplantar keratoderma-esophageal carcinoma syndrome  
 Papillon-Lefevre disease +   
 Patel Bixler Syndrome 
 Porokeratosis 2, Palmar, Plantar, and Disseminated Type 
 Powell Venencie Gordon syndrome 
 punctate palmoplantar keratoderma +   
 Schopf-Schulz-Passarge syndrome  
 Stern Lubinsky Durrie Syndrome 
 Vohwinkel syndrome  

Synonyms
Exact Synonyms: Hyperkeratosis Palmaris et Plantaris ;   Keratosis Palmaris et Plantaris ;   Palmoplantar Keratoderma ;   Palmoplantar Keratodermas ;   Palmoplantar Keratoses ;   palmo-plantar keratodermas
Narrow Synonyms: Unna-Thost disease ;   Unna-Thost keratoderma ;   Unna-Thost syndrome
Primary IDs: MESH:D007645
Alternate IDs: OMIA:001327
Xrefs: EFO:1000745 ;   GARD:8167 ;   ICD10CM:L85.2 ;   NCI:C34748
Definition Sources: http://en.wikipedia.org/wiki/Palmoplantar_keratoderma "DO" "DO"

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