adisease

Showing entry for Ullrich congenital muscular dystrophy 1

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD008411
Disease Name	Ullrich congenital muscular dystrophy 1
Disease CUI Id	C0410179
MeSH Codes	C23 C16 C05 C10
Disease Class Name	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System 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
P02751	BXGT005943	Fibronectin	2335	reviewed	Signaling
P04275	BXGT006180	von Willebrand factor	7450	reviewed	Enzyme modulator
P36969	BXGT009949	Phospholipid hydroperoxide glutathione peroxidase	2879	reviewed	Enzyme
Q92900	BXGT019392	Regulator of nonsense transcripts 1	5976	reviewed	Enzyme
Q96Q15	BXGT025610	Serine/threonine-protein kinase SMG1	23049	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}