aplasia/hypoplasia of the sacrum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Aplasia or developmental hypoplasia of the sacral bone. (Human Phenotype Ontology, HP_0008517)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008517
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Genes

8 genes associated with the aplasia/hypoplasia of the sacrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FANCB Fanconi anemia, complementation group B
FUCA1 fucosidase, alpha-L- 1, tissue
FUZ fuzzy planar cell polarity protein
MNX1 motor neuron and pancreas homeobox 1
POC1A POC1 centriolar protein A
ROR2 receptor tyrosine kinase-like orphan receptor 2
RPS19 ribosomal protein S19
VANGL1 VANGL planar cell polarity protein 1