neonatal epiphyseal stippling Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of abnormal punctate (speckled, dot-like) calcifications in one or more epiphyses during the neonatal period. (Human Phenotype Ontology, HP_0005756)
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1 genes associated with the neonatal epiphyseal stippling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha