Showing entry for Leukodystrophy, Hypomyelinating, 2

General Disease Information
BXGD Id	BXGD014224
Disease Name	Leukodystrophy, Hypomyelinating, 2
Disease CUI Id	C1837355
MeSH Codes	C16   C18   C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; 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