I I- I0 I1 I2 I3 I4 I5 I6 I7 I8 I9 IA IB IC ID IE IF IG IH II IK IL IM IN IO IP IQ IR IS IT IU IV IX
inborn biological transport disorder
[condition in which there is a deviation or interruption in the movement of materials (including biochemical substances and drugs) through a biological system at the cellular level; the defects in transport can occur within intracellular and extracellular compartments. ( CSP )]
UMLS (CSP) C0596765- Disease or Syndrome
Relation/PAR: Congenital Metabolic Disorder
Relation/CHD: Bartter's Disease
cystic fibrosis
De Toni-Debre-Fanconi Syndrome
inborn renal tubular transport disorder
hereditary carnitine deficiency myopathy
vitamin B12 transport defect
familial hypophosphatemia in rickets
congenital sucrose isomaltose malabsorption
cystic fibrosis
De Toni-Debre-Fanconi Syndrome
inborn renal tubular transport disorder
hereditary carnitine deficiency myopathy
vitamin B12 transport defect
familial hypophosphatemia in rickets
congenital sucrose isomaltose malabsorption
  |
 home | Dictionaries  Armenian-English English-Armenian MeSH Feedback |  top |
| © 2008 -2011 Administrator | MEDINDEX.AM |