pitt-hopkins syndrome Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Pitt-Hopkins syndrome (PHS) is characterized by the association of intellectual deficit, characteristic facial dysmorphism and problems of abnormal and irregular breathing. (Orphanet Rare Disease Ontology, Orphanet_2896)
External Link http://www.omim.org/entry/610954
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Genes

1 genes associated with the pitt-hopkins syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
TCF4 transcription factor 4