Showing entry for Ciliary Motility Disorders



                               
General Disease Information
BXGD IdBXGD000571
Disease NameCiliary Motility Disorders
Disease CUI IdC0008780
MeSH Codes C16   C08   C09  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id HP:0002086  
Human Phenotype Ontology TermAbnormality of the respiratory system
Disease Ontology Id DOID:630   DOID:225  
Disease Ontology Class Namegenetic disease; syndrome
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
O94813 BXGT005337 Slit homolog 2 protein 9353 reviewed
P07437 BXGT006624 Tubulin beta chain 203068 reviewed Cellular structure
Q92834 BXGT019381 X-linked retinitis pigmentosa GTPase regulator 6103 reviewed
Q9BW19 BXGT020148 Kinesin-like protein KIFC1 3833 reviewed Cellular structure
Q9NRR6 BXGT021193 Phosphatidylinositol polyphosphate 5-phosphatase type IV 56623 reviewed
Q9UGP5 BXGT021689 DNA polymerase lambda 27343 reviewed Enzyme
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