Ontology Browser

Term:
Dowling-Degos disease (DOID:0060256)
Annotations: Rat: (4) Mouse: (4) Human: (4) Chinchilla: (4) Bonobo: (4) Dog: (4) Squirrel: (4)
Parent Terms Term With Siblings Child Terms
Absence of Fingerprints  
Actinic Prurigo  
Albinism +   
Annular Erythema 
arterial tortuosity syndrome  
Ataxia-Telangiectasia with Generalized Skin Pigmentation and Early Death 
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  
Collagenosis, Familial Reactive Perforating 
Congenital Erythroderma with Palmoplantar Keratoderma, Hypotrichosis, and Hyper-IgE  
Cutaneous Bullous Amyloidosis 
cutaneous porphyria  
cutis laxa +   
Dermatopathia Pigmentosa Reticularis  
dermatosis papulosa nigra 
Dowling-Degos disease +   
A pigmentation disease characterized by a reticulate pattern of abnormally dark skin coloring, particularly in the body's folds and creases. (DO)
dyschromatosis universalis hereditaria +   
dyskeratosis congenita +   
ectodermal dysplasia +   
Ehlers-Danlos syndrome +   
epidermolysis bullosa +   
epidermolytic hyperkeratosis +   
erythrokeratodermia variabilis +   
Erythrokeratodermia with Ataxia  
Familial Dyskeratotic Comedones 
Gerodermia Osteodysplastica  
Granulosis Rubra Nasi 
Hailey-Hailey disease  
Hepatic Porphyrias +   
Hereditary Autoinflammatory Diseases +   
hereditary mucosal leukokeratosis  
Hereditary Sclerosing Poikiloderma +   
Histiocytic Dermatoarthritis 
Hyaluronan Metabolism, Defect in 
Hyperkeratosis-Hyperpigmentation Syndrome 
hyperpigmentation of eyelid 
Hyperpigmentation of Fuldauer and Kuijpers 
Hyperpigmentation, Familial Progressive +   
ichthyosis vulgaris +   
Isolated Osteopoikilosis 
Juvenile Spring Eruption of Ears 
Keratolytic Winter Erythema  
keratosis follicularis +   
Keratosis Follicularis Spinulosa Decalvans, X-Linked  
Keratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma  
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
lichen disease +   
lipoid proteinosis  
Melanosis +   
Melanosis, Universal 
monilethrix +   
Muir-Torre syndrome  
Multiform Ventricular Extrasystoles with Short Stature, Hyperpigmentation and Microcephaly 
Multiple Noduli Cutanei with Urinary Tract Abnormalities 
Oculotrichodysplasia 
orofaciodigital syndrome IX  
palmoplantar keratosis +   
Parana Hard Skin Syndrome 
parapsoriasis +   
Patterson Pseudoleprechaunism 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 
Pityriasis +   
Plasminogen Deficiency, Type I  
porokeratosis +   
primary cutaneous amyloidosis +   
Progressive Osseous Heteroplasia  
Progressive Vitiligo with Mental Retardation and Urethral Duplication 
Prolidase Deficiency  
pseudoxanthoma elasticum +   
psoriasis +   
Reticulate Pigmentary Disorder, with Systemic Manifestations  
Rothmund-Thomson syndrome +   
seborrheic dermatitis +   
Sjogren-Larsson syndrome +   
Skin Fragility-Woolly Hair Syndrome  
Stiff Skin Syndrome  
Storm Syndrome 
Systemic Hyalinosis  
Trichothiodystrophy Syndromes +   
Vohwinkel Syndrome, Variant Form  
X-linked ichthyosis +   
xeroderma pigmentosum +   

Synonyms
Exact Synonyms: DDD ;   DDD1 ;   Dowling-Degos disease 1 ;   Dowling-Degos-Kitamura disease ;   RPK ;   acropigmentatio reticularis ;   dark dot disease ;   reticular pigment anomaly of flexures
Primary IDs: MESH:C562924
Alternate IDs: OMIM:179850 ;   RDO:0012431
Xrefs: GARD:9775 ;   OMIM:PS179850 ;   ORDO:79145
Definition Sources: http://en.wikipedia.org/wiki/Reticular_pigmented_anomaly_of_the_flexures, http://ghr.nlm.nih.gov/condition/dowling-degos-disease

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.