Acromicric Dysplasia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Acromicric dysplasia is a rare bone dysplasia characterized by short stature, short hands and feet, mild facial dysmorphism, and characteristic X-ray abnormalities of the hands. (Orphanet Rare Disease Ontology, Orphanet_969)
External Link https://www.disgenet.org/browser/0/1/0/C0265287
Similar Terms
Downloads & Tools

Genes

15 genes associated with the disease Acromicric Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADAMTS1 ADAM metallopeptidase with thrombospondin type 1 motif, 1
ADAMTS10 ADAM metallopeptidase with thrombospondin type 1 motif, 10
ADAMTSL2 ADAMTS-like 2
EGF epidermal growth factor
FBN1 fibrillin 1
HERC2 HECT and RLD domain containing E3 ubiquitin protein ligase 2
HSPB3 heat shock 27kDa protein 3
LTBP3 latent transforming growth factor beta binding protein 3
MAGEL2 melanoma antigen family L2
MKRN3 makorin ring finger protein 3
NDN necdin, melanoma antigen (MAGE) family member
NPAP1 nuclear pore associated protein 1
SMAD2 SMAD family member 2
SNRPN small nuclear ribonucleoprotein polypeptide N
TGFB1 transforming growth factor, beta 1