Showing entry for Arthrogryposis multiplex congenita, distal, X-linked

General Disease Information
BXGD Id	BXGD014697
Disease Name	Arthrogryposis multiplex congenita, distal, X-linked
Disease CUI Id	C1844934
MeSH Codes	C16   C05
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations