nablus mask-like facial syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome is a rare microdeletion syndrome associated with a distinct facial appearance. (Orphanet Rare Disease Ontology, Orphanet_178303)
External Link http://www.omim.org/entry/608156
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Genes

1 genes associated with the nablus mask-like facial syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
NMLFS Nablus mask-like facial syndrome