adisease

Showing entry for Alobar Holoprosencephaly

　　　　　　　　　　　　　　　　

General Disease Information
BXGD Id	BXGD008671
Disease Name	Alobar Holoprosencephaly
Disease CUI Id	C0431363
MeSH Codes	C16 C05 C10
Disease Class Name	Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
Semantic Type	Congenital Abnormality
Human Phenotype Ontology Id	HP:0000707
Human Phenotype Ontology Term	Abnormality of the nervous system
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
P10070	BXGT007534	Zinc finger protein GLI2	2736	reviewed
Q15465	BXGT013573	Sonic hedgehog protein	6469	reviewed
Q4KMG0	BXGT014850	Cell adhesion molecule-related/down-regulated by oncogenes	50937	reviewed
Q15583	BXGT024027	Homeobox protein TGIF1	7050	reviewed	Enzyme
Q13635	BXGT024910	Protein patched homolog 1	5727	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}