Human genes for Pallister-Hall syndrome
Pallister-Hall syndrome [DOID:9248]
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.
Synonyms: Pallister-Hall syndrome, DOID:9248, PallisterHall syndrome, Pallister-Hall disease, Pallister-Hall disorder ...
Linkouts: OMIM