Dataset | HPO Gene-Disease Associations |
Category | disease or phenotype associations |
Type | phenotype |
Description | Intrauterine growth retardation that is at least 2 standard deviations (SD) below average, but not as low as 3 SD, corrected for sex and gestational age. (Human Phenotype Ontology, HP_0008883) |
External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0008883 |
Similar Terms | |
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1 genes associated with the mild intrauterine growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Symbol | Name |
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NSDHL | NAD(P) dependent steroid dehydrogenase-like |