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

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