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MCID: RTT001
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Ritter's Disease malady |
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Sources: 6Disease Ontology, 22MalaCards See all sources Export this MalaCard |
Disease Ontology: A commensal bacterial infectious disease that is characterized by widespread erythema, peeling, and necrosis of the skin, that is caused by a toxin produced by a bacterium of the genus staphylococcus (s. aureus). the infection has symptoms redness of skin, has symptom fluid-filled blister formation, has symptom fever and has symptom irritability.6
MalaCards: Ritter's Disease, also known as pemphigus neonatorum, is related to toxic epidermal necrolysis and netherton syndrome, and has symptoms including fluid-filled blister formation, fever and irritability. An important gene associated with Ritter's Disease is AGR3 (anterior gradient 3 homolog (Xenopus laevis)). The compounds pd 145065 and sitaxsentan have been mentioned in the context of this disorder. Affiliated tissues include skin. |
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Sources: 6Disease Ontology, 43UMLS, 8DISEASES, 19ICD9CM, 27NCIt, 40SNOMED-CT, 24MeSH See all sources |
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Sources: 6Disease Ontology See all sources |
Symptoms: fluid-filled blister formation, fever, irritability.6
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Sources: 4CenterWatch, 29NIH Clinical Center, 5ClinicalTrials See all sources |
Approved drugs:Search CenterWatch for ritter's disease Drug clinical trials:Search ClinicalTrials for ritter's disease Search NIH Clinical Center for ritter's disease Search CenterWatch for ritter's disease |
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Sources: 22MalaCards See all sources |
MalaCards organs/tissues related to ritter's disease:22Skin
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Sources: 1BioGPS See all sources |
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Sources: 32Novoseek , 9DrugBank, 18HMDB See all sources |
Compounds related to ritter's disease according to GeneDecks:(show all 22)
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Sources: 12Gene Ontology See all sources |
Cellular components related to ritter's disease according to GeneDecks:
Biological processes related to ritter's disease according to GeneDecks:
Molecular functions related to ritter's disease according to GeneDecks:
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