adisease

Showing entry for Congenital Myotonic Dystrophy

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD008421
Disease Name	Congenital Myotonic Dystrophy
Disease CUI Id	C0410226
MeSH Codes	C16 C05 C10
Disease Class Name	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
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
P05231	BXGT006345	Interleukin-6	3569	reviewed
P49711	BXGT010728	Transcriptional repressor CTCF	10664	reviewed	Transcription factor
P52952	BXGT010966	Homeobox protein Nkx-2.5	1482	reviewed	Transcription factor
Q09013	BXGT013023	Myotonin-protein kinase	1760	reviewed	Kinase
Q9NR56	BXGT021179	Muscleblind-like protein 1	4154	reviewed	Nucleic acid binding

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}