PedAM
Pediatric Disease Annotations & Medicines
| Disease | neuropathy |
| Phenotype | C0162565|acute intermittent porphyria |
| Sentences | 1 |
| PubMedID- 21855406 | The neuropathy associated with acute intermittent porphyria (aip) occurs due to mutation involving the enzyme porphobilinogen deaminase (pbgd) and is characterised by motor-predominant features. |
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