Showing entry for Schwartz-Lelek syndrome

General Disease Information
BXGD Id	BXGD005504
Disease Name	Schwartz-Lelek syndrome
Disease CUI Id	C0265292
MeSH Codes	C16   C05
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations