adisease

Showing entry for CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (disorder)

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD017307
Disease Name	CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (disorder)
Disease CUI Id	C2675746
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
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
O76039	BXGT005171	Cyclin-dependent kinase-like 5	6792	reviewed	Kinase
P10145	BXGT007542	Interleukin-8	3576	reviewed	Signaling
P32320	BXGT009622	Cytidine deaminase	978	reviewed	Enzyme
P42262	BXGT010294	Glutamate receptor 2	2891	reviewed	Ion channel

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}