congenital cataracts, facial dysmorphism, and neuropathy Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/604168
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Genes

1 genes associated with the congenital cataracts, facial dysmorphism, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CTDP1 CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1