Cartilage-hair hypoplasia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_14773)
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1 genes/proteins associated with the disease Cartilage-hair hypoplasia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
RMRP RNA component of mitochondrial RNA processing endoribonuclease 2.88009