| 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 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the pitt-hopkins syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| TCF4 | transcription factor 4 |
