Acromicric dysplasia Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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 http://www.omim.org/entry/102370
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Genes

1 genes associated with the Acromicric dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
FBN1 fibrillin 1