Showing entry for Schnyder crystalline corneal dystrophy



                               
General Disease Information
BXGD IdBXGD006181
Disease NameSchnyder crystalline corneal dystrophy
Disease CUI IdC0271287
MeSH Codes C16   C11  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id HP:0000478  
Human Phenotype Ontology TermAbnormality of the eye
Disease Ontology Id DOID:7  
Disease Ontology Class Namedisease of anatomical entity
Disorder Network disorder-protein-compound-food associations