adisease

Showing entry for Congenital absence of parathyroid gland

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD012451
Disease Name	Congenital absence of parathyroid gland
Disease CUI Id	C1321907
MeSH Codes	C16 C19
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Endocrine System Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0000818
Human Phenotype Ontology Term	Abnormality of the endocrine system
Disease Ontology Id	DOID:630 DOID:7
Disease Ontology Class Name	genetic disease; disease of anatomical entity
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
Q8NB49	BXGT024770	Phospholipid-transporting ATPase IG	286410	reviewed	Transporter

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}