adisease

Showing entry for Autosomal dominant hypophosphatemic rickets

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD007519
Disease Name	Autosomal dominant hypophosphatemic rickets
Disease CUI Id	C0342642
MeSH Codes	C16 C18 C13 C05 C12
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Musculoskeletal Diseases; Male Urogenital 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

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
O94907	BXGT005340	Dickkopf-related protein 1	22943	reviewed
P01270	BXGT005746	Parathyroid hormone	5741	reviewed
P22413	BXGT008764	Ectonucleotide pyrophosphatase/phosphodiesterase family member 1	5167	reviewed	Enzyme
P35222	BXGT009799	Catenin beta-1	1499	reviewed
Q86Z14	BXGT017639	Beta-klotho	152831	reviewed	Enzyme
Q96BR1	BXGT019627	Serine/threonine-protein kinase Sgk3	23678	reviewed

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}