PedAM
Pediatric Disease Annotations & Medicines
| Disease | cerebellar hypoplasia |
| Phenotype | C0026847|spinal muscular atrophy |
| Sentences | 2 |
| PubMedID- 25609612 | The spinal muscular atrophy with pontocerebellar hypoplasia gene vrk1 regulates neuronal migration through an amyloid-beta precursor protein-dependent mechanism. |
| PubMedID- 23284067 | Objectives: pontocerebellar hypoplasia with spinal muscular atrophy, also known as pch1, is a group of autosomal recessive disorders characterized by generalized muscle weakness and global developmental delay commonly resulting in early death. |
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