adisease

Showing entry for Mutilating keratoderma

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD005591
Disease Name	Mutilating keratoderma
Disease CUI Id	C0265964
MeSH Codes	C23 C16 C17 C05 C10 C09
Disease Class Name	Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id
Human Phenotype Ontology Term
Disease Ontology Id	DOID:630
Disease Ontology Class Name	genetic disease
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
P08195	BXGT006745	4F2 cell-surface antigen heavy chain	6520	reviewed	Transporter
P10415	BXGT007567	Apoptosis regulator Bcl-2	596	reviewed	Signaling
P29033	BXGT009308	Gap junction beta-2 protein	2706	reviewed	Cell-cell junction
P48506	BXGT010635	Glutamate--cysteine ligase catalytic subunit	2729	reviewed	Enzyme
P48507	BXGT010636	Glutamate--cysteine ligase regulatory subunit	2730	reviewed	Enzyme
Q01650	BXGT012603	Large neutral amino acids transporter small subunit 1	8140	reviewed	Transporter
Q9Y4K0	BXGT022280	Lysyl oxidase homolog 2	4017	reviewed

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}