Aplasia/Hypoplasia Of The Earlobes Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Absence or underdevelopment of the ear lobes. (Human Phenotype Ontology, HP_0009906)
External Link https://www.disgenet.org/browser/0/1/0/C1851792
Similar Terms
Downloads & Tools

Genes

11 genes associated with the disease Aplasia/Hypoplasia Of The Earlobes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CHD7 chromodomain helicase DNA binding protein 7
COL3A1 collagen, type III, alpha 1
FGFR2 fibroblast growth factor receptor 2
FLI1 Fli-1 proto-oncogene, ETS transcription factor
HBA1 hemoglobin, alpha 1
HBA2 hemoglobin, alpha 2
LMNA lamin A/C
PCNT pericentrin
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
VPS13B vacuolar protein sorting 13 homolog B (yeast)
ZMPSTE24 zinc metallopeptidase STE24