adisease

Showing entry for Congenital musculoskeletal anomalies

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD003428
Disease Name	Congenital musculoskeletal anomalies
Disease CUI Id	C0151491
MeSH Codes	C16 C05
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
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
P00519	BXGT005570	Tyrosine-protein kinase ABL1	25	reviewed	Kinase
P02545	BXGT005889	Prelamin-A/C	4000	reviewed
P13631	BXGT007929	Retinoic acid receptor gamma	5916	reviewed	Nuclear receptor
P37173	BXGT009970	TGF-beta receptor type-2	7048	reviewed	Kinase
P37840	BXGT010015	Alpha-synuclein	6622	reviewed	Transporter
Q01968	BXGT012626	Inositol polyphosphate 5-phosphatase OCRL-1	4952	reviewed	Enzyme
Q99958	BXGT023732	Forkhead box protein C2	2303	reviewed	Transcription factor

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}