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Term:
juvenile xanthogranuloma (DOID:4424)
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Parent Terms Term With Siblings Child Terms
Achenbach syndrome 
Acneiform Eruptions +   
adult xanthogranuloma 
allergic cutaneous vasculitis +   
ancylostomiasis +  
angioedema +   
Borrone Di Rocco Crovato Syndrome  
Boudhina Yedes Khiari syndrome 
breast disease +   
C Syndrome  
cercarial dermatitis 
chancroid +  
chronic ulcer of skin +   
coenurosis 
contagious pustular dermatitis 
Cutaneous Fistula 
cutaneous lupus erythematosus +   
cutaneous mycosis +   
cutis laxa +   
Dermal Fibrosis  
dermatitis +   
Dermatoleukodystrophy 
dermatomyositis +   
dipetalonemiasis 
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
Ectodermal Dysplasia-Skin Fragility Syndrome  
Eczematous Skin Diseases +   
Elastosis Perforans Serpiginosa 
Elliott Ludman Teebi Syndrome 
endometriosis in scar of skin 
epidermal nevus +   
epidermolytic hyperkeratosis +   
Erdheim-Chester disease 
Erythema +   
erythematosquamous dermatosis 
exanthem +   
FACES Syndrome 
facial dermatosis +   
Facial Ectodermal Dysplasia  
filariasis +   
Flynn Aird Syndrome 
Focal Facial Dermal Dysplasia 4  
Foot Diseases +   
Genetic Skin Diseases +   
hair disease +   
hand dermatosis +  
hemophagocytic lymphohistiocytosis +   
Hernandez Fragoso Syndrome 
ichthyosis +   
Infectious Skin Diseases +   
juvenile xanthogranuloma 
Benign disorder of infants and children caused by proliferation of HISTIOCYTES, macrophages found in tissues. These histiocytes, usually lipid-laden non-Langerhans cells, form multiple yellow-red nodules most often in the skin, the eye, and sometimes in the viscera. Patients appear to have normal lipid metabolism and are classified as a normolipemic non-Langerhans cell histiocytosis.
keratosis +   
Kimura disease 
leg dermatosis 
lipomatosis +   
localized scleroderma +   
loiasis 
Macroepiphyseal Dysplasia, McAlister Coe Type 
MASS Syndrome  
mastocytosis +   
Median Cleft Lip, Corpus Callosum, Lipoma, and Skin Polyps 
Mental Retardation, Joint Hypermobility, and Skin Laxity, with or without Metabolic Abnormalities 
Metabolic Skin Diseases +   
mongolian spot 
Morgellons Disease 
multicentric reticulohistiocytosis 
multiple cutaneous and mucosal venous malformations  
nail disease +   
necrobiosis lipoidica 
Necrobiotic Disorders +  
Necrolytic Migratory Erythema 
Nephrogenic Fibrosing Dermopathy  
Niemann-Pick disease +   
noninfectious dermatoses of eyelid +  
otulipenia  
Papulosquamous Skin Diseases +   
photosensitivity disease +   
pigmentation disease +   
Prurigo  
Pruritus +   
Pseudoatrophoderma Colli 
reactive cutaneous fibrous lesion +  
reticulohistiocytic granuloma 
rosacea +   
Roy Maroteaux Kremp Syndrome 
scalp dermatosis +   
sea-blue histiocyte syndrome  
sebaceous gland disease +   
Sinus Histiocytosis +   
Skin Abnormalities +   
skin atrophy 
Skin Neoplasms +   
skin sarcoidosis 
strongyloidiasis  
sweat gland disease +   
systemic scleroderma +   
tyrosinemia type II  
Upton Young Syndrome 
urticaria +   
vascular skin disease +   
verruciform xanthoma of skin 
vesiculobullous skin disease +   
Wegener's granulomatosis +   

Synonyms
Exact Synonyms: Juvenile Xanthogranulomas ;   Juvenile Xanthoma ;   Juvenile Xanthomas ;   Multiple eruptive juvenile xanthogranuloma ;   Naevoxanthoendothelioma ;   Nevoxanthoendothelioma ;   Nevoxanthoendotheliomas ;   Xanthoma neviforme
Primary IDs: MESH:D014972 ;   RDO:0006835
Definition Sources: MESH:D014972

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