Showing entry for Prenatal movement abnormality

General Disease Information
BXGD Id	BXGD015061
Disease Name	Prenatal movement abnormality
Disease CUI Id	C1849510
MeSH Codes
Disease Class Name
Semantic Type	Finding
Human Phenotype Ontology Id	HP:0001197
Human Phenotype Ontology Term	Abnormality of prenatal development or birth
Disease Ontology Id
Disease Ontology Class Name
Disorder Network	disorder-protein-compound-food associations