aplasia/hypoplasia of the spleen Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the spleen. (Human Phenotype Ontology, HP_0010451)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010451
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13 genes associated with the aplasia/hypoplasia of the spleen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIRE autoimmune regulator
DNAI1 dynein, axonemal, intermediate chain 1
FAM111A family with sequence similarity 111, member A
GDF1 growth differentiation factor 1
MKS1 Meckel syndrome, type 1
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NEK8 NIMA-related kinase 8
NPHP3 nephronophthisis 3 (adolescent)
RPSA ribosomal protein SA
STIM1 stromal interaction molecule 1
STRA6 stimulated by retinoic acid 6
WNT3 wingless-type MMTV integration site family, member 3
ZIC3 Zic family member 3