Showing entry for Sjogren-Larsson Syndrome



                               
General Disease Information
BXGD IdBXGD002674
Disease NameSjogren-Larsson Syndrome
Disease CUI IdC0037231
MeSH Codes C16   C18   C17  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:630  
Disease Ontology Class Namegenetic disease
Disorder Network disorder-protein-compound-food associations