adisease

Showing entry for KLIPPEL-FEIL SYNDROME, AUTOSOMAL DOMINANT

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD016065
Disease Name	KLIPPEL-FEIL SYNDROME, AUTOSOMAL DOMINANT
Disease CUI Id	C1861689
MeSH Codes	C16 C05
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic Type	Disease or Syndrome
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630 DOID:7 DOID:225 DOID:0080015
Disease Ontology Class Name	genetic disease; disease of anatomical entity; syndrome; physical disorder
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
P25440	BXGT009044	Bromodomain-containing protein 2	6046	reviewed	Epigenetic regulator

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}