Showing entry for Amelogenesis Imperfecta, Hypomaturation Type, Iia2

General Disease Information
BXGD Id	BXGD017311
Disease Name	Amelogenesis Imperfecta, Hypomaturation Type, Iia2
Disease CUI Id	C2675858
MeSH Codes	C16   C07
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic 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