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Ontology Browser

Parent Terms Term With Siblings Child Terms
keratosis +     
acquired hyperkeratosis 
acrokeratosis verruciformis  
actinic keratosis +   
Actinic Prurigo  
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 
orofaciodigital syndrome IX  
palmoplantar keratosis +   
A keratosis characterized by abnormal thickening of the palms and the soles. (DO)
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 +   
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 +   

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: "DO" "DO"

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