Human genes for Jacobsen Syndrome
Jacobsen Syndrome [DOID:0111723]
A chromosomal deletion syndrome that is characterized by growth retardation, psychomotor retardation, distinctive facial features, skeletal abnormalities, and isoimmune thrombocytopenia that has_material_basis_in deletion of terminal chromosome 11q.
Synonyms: Jacobsen Syndrome, DOID:0111723, Jacobsen disease, Jacobsen disorder, Jacobsen Syndromes ...