| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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://ctdbase.org/detail.go?type=disease&acc=MESH:C537403 |
| Similar Terms | |
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3 genes/proteins associated with the disease Pitt-Hopkins syndrome from the curated CTD Gene-Disease Associations dataset.
