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Term:
Parent Terms Term With Siblings Child Terms
skin disease +     
2,4-Dienoyl-CoA Reductase Deficiency  
Acetyl-Coa Carboxylase Deficiency  
Achenbach syndrome 
Acneiform Eruptions +   
adiaspiromycosis 
allergic cutaneous vasculitis +   
alpha-methylacyl-CoA racemase deficiency  
ancylostomiasis +  
angioedema +   
Apolipoprotein A-I, Deficiency of +   
APOLIPOPROTEIN A-II DEFICIENCY  
Apolipoprotein E, Deficiency or Defect of +   
Barth syndrome +   
Boudhina Yedes Khiari syndrome 
breast disease +   
carnitine palmitoyltransferase I deficiency  
carnitine palmitoyltransferase II deficiency +   
Carnitine-Acylcarnitine Translocase Deficiency  
cercarial dermatitis 
cerebrotendinous xanthomatosis  
chancroid +  
Cholesteryl Ester Transfer Protein Deficiency  
chronic ulcer of skin +   
chylomicron retention disease  
coenurosis 
Congenital Lp(A) Deficiency  
contagious pustular dermatitis 
Cutaneous Fistula 
cutaneous lupus erythematosus +   
cutis laxa +   
Cytosolic Acetoacetyl-CoA Thiolase Deficiency  
D-bifunctional protein deficiency  
Dermal Fibrosis  
dermatitis +   
Dermatoleukodystrophy 
dermatomyositis +   
Desmosterolosis  
dipetalonemiasis 
Duplication of Eyebrows with Stretchable Skin and Syndactyly 
Dyslipidemias +   
Ectodermal Dysplasia-Skin Fragility Syndrome  
Eczematous Skin Diseases +   
Elastosis Perforans Serpiginosa 
Elliott Ludman Teebi Syndrome 
endometriosis in scar of skin 
epidermal nevus +   
epidermolytic hyperkeratosis +   
Erythema +   
erythematosquamous dermatosis 
exanthem +   
FACES Syndrome 
facial dermatosis +   
Facial Ectodermal Dysplasia  
familial combined hyperlipidemia +   
familial hyperlipidemia +   
familial lipoprotein lipase deficiency +   
filariasis +   
Flynn Aird Syndrome 
Focal Facial Dermal Dysplasia 4  
Foot Diseases +   
Genetic Skin Diseases +   
Glycosylphosphatidylinositol Deficiency +   
granulomatosis with polyangiitis +   
hair disease +   
hand dermatosis +  
hemorrhoid +   
Hepatic Lipase Deficiency  
Hernandez Fragoso Syndrome 
hyperlipoproteinemia type IV  
Hypertriglyceridemia, Transient Infantile  
hypolipoproteinemia +   
ichthyosis +   
Infectious Skin Diseases +   
juvenile xanthogranuloma 
keratosis +   
Kimura disease 
leg dermatosis 
Lipase Deficiency Combined  
lipid storage disease +   
lipodystrophy +   
lipoid proteinosis  
lipomatosis +   
A disorder characterized by the accumulation of encapsulated or unencapsulated tumor-like fatty tissue resembling LIPOMA.
localized scleroderma +   
loiasis 
Long-Chain 3-hydroxyacyl-CoA Dehydrogenase Deficiency +   
Macroepiphyseal Dysplasia, McAlister Coe Type 
MASS Syndrome  
mastocytosis +   
Median Cleft Lip, Corpus Callosum, Lipoma, and Skin Polyps 
medium chain acyl-CoA dehydrogenase deficiency  
MEND SYNDROME  
Mental Retardation, Joint Hypermobility, and Skin Laxity, with or without Metabolic Abnormalities 
Metabolic Skin Diseases +   
mongolian spot 
Morgellons Disease 
multicentric reticulohistiocytosis 
multiple congenital anomalies-hypotonia-seizures syndrome +   
multiple cutaneous and mucosal venous malformations  
Myopathy with Abnormal Lipid Metabolism  
nail disease +   
necrobiosis lipoidica 
Necrobiotic Disorders +  
Necrolytic Migratory Erythema 
Nephrogenic Fibrosing Dermopathy  
neutral lipid storage disease +   
noninfectious dermatoses of eyelid +  
Opitz Trigonocephaly Syndrome  
otulipenia  
Pancreatic Lipase Deficiency  
Papulosquamous Skin Diseases +   
peroxisomal acyl-CoA oxidase deficiency  
PEROXISOMAL FATTY ACYL-COA REDUCTASE 1 DISORDER  
phaeohyphomycosis +  
Phospholipase A2, Group IVA, Deficiency of  
photosensitivity disease +   
pigmentation disease +   
Prurigo  
Pruritus +   
Pseudoatrophoderma Colli 
reactive cutaneous fibrous lesion +  
Refsum disease +   
rosacea +   
Roy Maroteaux Kremp Syndrome 
scalp dermatosis +   
sebaceous gland disease +   
short chain acyl-CoA dehydrogenase deficiency  
sitosterolemia  
Skin Abnormalities +   
skin atrophy 
Skin Neoplasms +   
skin sarcoidosis 
Smith-Lemli-Opitz syndrome +   
steroid inherited metabolic disorder +   
strongyloidiasis  
sweat gland disease +   
syndromic X-linked intellectual disability type 10  
systemic scleroderma +   
Ter Haar Syndrome  
Triglyceride Storage Disease, Type I 
Triglyceride Storage Disease, Type II 
tyrosinemia type II  
Upton Young Syndrome 
urticaria +   
vascular skin disease +   
verruciform xanthoma of skin 
very long chain acyl-CoA dehydrogenase deficiency  
vesiculobullous skin disease +   
xanthomatosis +   

Synonyms
Exact Synonyms: Lipomatoses
Primary IDs: MESH:D008068 ;   RDO:0000730
Definition Sources: MESH:D008068

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