Absent Radius Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Missing radius bone associated with congenital failure of development. (Human Phenotype Ontology, HP_0003974)
External Link https://www.disgenet.org/browser/0/1/0/C1405984
Similar Terms
Downloads & Tools

Genes

23 genes associated with the disease Absent Radius in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CHN1 chimerin 1
COL25A1 collagen, type XXV, alpha 1
DONSON downstream neighbor of SON
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
F10 coagulation factor X
FANCA Fanconi anemia, complementation group A
FANCB Fanconi anemia, complementation group B
FANCC Fanconi anemia, complementation group C
FANCD2 Fanconi anemia, complementation group D2
FANCE Fanconi anemia, complementation group E
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FLNB filamin B, beta
GLI3 GLI family zinc finger 3
LMBR1 limb development membrane protein 1
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
RBM8A RNA binding motif protein 8A
RECQL4 RecQ protein-like 4
SALL4 spalt-like transcription factor 4
SF3B4 splicing factor 3b, subunit 4, 49kDa
TBX3 T-box 3
ZIC3 Zic family member 3