|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||The presence of abnormal punctate (speckled, dot-like) calcifications in one or more epiphyses during the neonatal period. (Human Phenotype Ontology, HP_0005756)|
|Downloads & Tools|
1 genes associated with the neonatal epiphyseal stippling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|PRKAR1A||protein kinase, cAMP-dependent, regulatory, type I, alpha|