Acromicric dysplasia Gene Set

Dataset CTD 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)
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3 genes/proteins associated with the disease Acromicric dysplasia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
SMAD2 SMAD family member 2 2.88009
ADAMTSL2 ADAMTS-like 2 2.88009
TGFB1 transforming growth factor, beta 1 2.88009