PedAM
Pediatric Disease Annotations & Medicines
| Disease | tic disorder |
| Phenotype | C0268483|tyrosinemia |
| Sentences | 1 |
| PubMedID- 21107780 | More than ten genetic disorders (including tyrosinemia neonatal or type i, homocystnuria, 2-ch3-3-hydroxybutyric aciduria, galactosemia, hereditary fructose intolerance, cytrulinemia type ii, biotinidase deficiency, wilson disease, and lysosomal storage disorders) were suspected and subsequently excluded during the long-term hospitalizations in our referral metabolic center. |
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