adisease

Showing entry for Sacral agenesis

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD007680
Disease Name	Sacral agenesis
Disease CUI Id	C0344490
MeSH Codes	C23 C16 C10
Disease Class Name	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0000924
Human Phenotype Ontology Term	Abnormality of the skeletal system
Disease Ontology Id
Disease Ontology Class Name
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
O15178	BXGT004135	T-box transcription factor T	6862	reviewed	Transcription factor
P13500	BXGT007916	C-C motif chemokine 2	6347	reviewed	Signaling
P21817	BXGT008693	Ryanodine receptor 1	6261	reviewed	Ion channel
Q03431	BXGT012714	Parathyroid hormone/parathyroid hormone-related peptide receptor	5745	reviewed	G-protein coupled receptor
Q15465	BXGT013573	Sonic hedgehog protein	6469	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}