PedAM
Pediatric Disease Annotations & Medicines
| Disease | n syndrome |
| Phenotype | C0078918|oculocutaneous albinism |
| Sentences | 1 |
| PubMedID- 25690523 | Conclusion: the new data provided here may be useful for further genotype correlations in syndromes with oculocutaneous albinism, especially of autosomal dominant inheritance. |
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