Secondary Growth Hormone Deficiency Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
External Link	https://www.disgenet.org/browser/0/1/0/C4024716
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Genes

11 genes associated with the disease Secondary Growth Hormone Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
ABCC8	ATP-binding cassette, sub-family C (CFTR/MRP), member 8
AIP	aryl hydrocarbon receptor interacting protein
CDH23	cadherin-related 23
GLI3	GLI family zinc finger 3
KCNJ11	potassium channel, inwardly rectifying subfamily J, member 11
MEN1	multiple endocrine neoplasia I
NF2	neurofibromin 2 (merlin)
PDGFB	platelet-derived growth factor beta polypeptide
SMARCB1	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
SUFU	suppressor of fused homolog (Drosophila)
UCP2	uncoupling protein 2 (mitochondrial, proton carrier)