adisease

Showing entry for Primary hypomagnesemia (disorder)

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD005950
Disease Name	Primary hypomagnesemia (disorder)
Disease CUI Id	C0268448
MeSH Codes	C23 C16 C18 C13 C12
Disease Class Name	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:0014667 DOID:630
Disease Ontology Class Name	disease of metabolism; genetic disease
Disorder Network	disorder-protein-compound-food associations

The disease-related target proteins

Proteins

Uniport Id	BXGT Id	Protein Name	Gene	Status	Protein Class
Uniport Id	BXGT Id	Protein name	Gene	Status	Protein class
P54710	BXGT011070	Sodium/potassium-transporting ATPase subunit gamma	486	reviewed	Transporter
Q9BX84	BXGT020161	Transient receptor potential cation channel subfamily M member 6	140803	reviewed	Kinase

The disease-related compounds

Compounds

BXGC Id	Compound Name	Structure	Molecular Weight	Number of targets^{?Number of times compound connecting the disease , higher numbers indicate the compound is more associated with the disease}

The disease-related foods

Foods

BXGF Id	Food Name	Scientific Name	Food Group	Number of compounds in food^{?Number of compounds in food that connecting disease, higher numbers indicate the more compounds in food are more associated with the dusease}