adisease

Showing entry for Congenital absence of breast

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD005604
Disease Name	Congenital absence of breast
Disease CUI Id	C0266009
MeSH Codes	C16
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0000769
Human Phenotype Ontology Term	Abnormality of the breast
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
O15119	BXGT004128	T-box transcription factor TBX3	6926	reviewed	Transcription factor
O43929	BXGT004638	Origin recognition complex subunit 4	5000	reviewed	Nucleic acid binding
O75496	BXGT005132	Geminin	51053	reviewed
P02545	BXGT005889	Prelamin-A/C	4000	reviewed
Q13415	BXGT013350	Origin recognition complex subunit 1	4998	reviewed	Nucleic acid binding
Q9Y4D7	BXGT022275	Plexin-D1	23129	reviewed
Q9Y6K9	BXGT022333	NF-kappa-B essential modulator	8517	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}