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Ontology Browser

Parent Terms Term With Siblings Child Terms
Blister +     
Actinic Prurigo  
Bullous Dystrophy, Hereditary Macular Type 
Cutaneous Photosensitivity and Colitis, Lethal 
epidermolysis bullosa acquisita 
epidermolysis bullosa dystrophica +   
epidermolysis bullosa simplex +   
Epidermolysis Bullosa with Deficiency of Galactosylhydroxylysyl Glucosyltransferase 
Epidermolysis Bullosa with Diaphragmatic Hernia 
Epidermolysis Bullosa, Lethal Acantholytic  
Epidermolysis Bullosa, Nonspecific, Autosomal Recessive  
Furcation Defects 
gingival disease +   
Hair Defect with Photosensitivity and Mental Retardation 
Hydroa Vacciniforme +  
hypotrichosis and recurrent skin vesicles  
Interstitial Lung Disease, Nephrotic Syndrome, and Epidermolysis Bullosa, Congenital  
junctional epidermolysis bullosa +   
Kindler syndrome  
A skin disease characterized by congenital blistering, skin atrophy, photosensitivity, skin fragility, and scaling. (DO)
Nephropathy with Pretibial Epidermolysis Bullosa and Deafness  
Papillon-Lefevre disease +   
Periapical Diseases +   
Periodontal Atrophy +   
Periodontal Cyst +   
periodontitis +   
photoallergic dermatitis +  
photosensitive epilepsy +  
photosensitive trichothiodystrophy +   
phototoxic dermatitis 
Pulmonary Bullae Causing Pneumothorax 
Tooth Loss 
Tooth Migration +  
Tooth Mobility 
UV-Induced Skin Damage  
UV-sensitive syndrome +   
xeroderma pigmentosum +   

Exact Synonyms: Bullous acrokeratotic poikiloderma of kindler and weary ;   Congenital bullous poikiloderma ;   KNDLRS ;   Kindler's syndrome ;   Poikiloderma, congenital, with bullae, weary type ;   Poikiloderma, hereditary acrokeratotic ;   hereditary acrokeratotic poikiloderma of Kindler-Weary ;   poikiloderma of Kindler
Primary IDs: MESH:C536321
Alternate IDs: OMIM:173650 ;   RDO:0001857
Xrefs: GARD:4391 ;   ORDO:306539
Definition Sources:,

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