adisease

Showing entry for Congenital absence of thymus

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD009825
Disease Name	Congenital absence of thymus
Disease CUI Id	C0685894
MeSH Codes	C20
Disease Class Name	Immune System Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0000818 HP:0002715 HP:0001626
Human Phenotype Ontology Term	Abnormality of the endocrine system; Abnormality of the immune system; Abnormality of the cardiovascular 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
O15353	BXGT004155	Forkhead box protein N1	8456	reviewed
P00813	BXGT005667	Adenosine deaminase	100	reviewed	Enzyme
Q96SD1	BXGT025929	Protein artemis	64421	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}