|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the pitt-hopkins syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
|TCF4||transcription factor 4|