Showing entry for Muscular atrophy, spinal, infantile chronic form

General Disease Information
BXGD Id	BXGD018008
Disease Name	Muscular atrophy, spinal, infantile chronic form
Disease CUI Id	C2931358
MeSH Codes	C16   C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630   DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
Disorder Network	disorder-protein-compound-food associations