Showing entry for Familial Partial Lipodystrophy, Type 1



                               
General Disease Information
BXGD IdBXGD013688
Disease NameFamilial Partial Lipodystrophy, Type 1
Disease CUI IdC1720859
MeSH Codes C18   C17  
Disease Class NameNutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id   
Human Phenotype Ontology Term
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease of anatomical entity
Disorder Network disorder-protein-compound-food associations