OBO ID: DOID:9248 |
Term Name: | Pallister-Hall syndrome | Search Ontology: | |
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Definition: | A syndrome that is characterized by hypothalamic hamartoma, pituitary dysfunction, central polydactyly, and visceral malformations and has_material_basis_in autosomal dominant heterozygous mutation in the GLI3 gene on chromosome 7p14. (3) | ||
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Ontology: | Human Disease ( DOID:9248 ) |
OTHER Pallister-Hall syndrome PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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