| Disease |
Page Type |
Author
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Date Assigned to Author
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Target Completion Date
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Author Content (Pending or Complete)
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Date Completed by Author |
Associate Editor
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Date of Last Editor Review
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Notes
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| Astrocytoma, IDH-mutant
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Disease
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| Oligodendroglioma, IDH-mutant and 1p/19q-codeleted
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Disease
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| Glioblastoma, IDH-wildtype
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Disease
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| Diffuse astrocytoma, MYB- or MYBL1-altered
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Disease
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| Angiocentric glioma
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Disease
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| Polymorphous low-grade neuroepithelial tumour of the young
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Disease
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| Diffuse low-grade glioma, MAPK pathway-altered
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Disease
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| Diffuse midline glioma, H3 K27-altered
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Disease
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| Diffuse hemispheric glioma, H3 G34-mutant
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Disease
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| Diffuse paediatric-type high-grade glioma, H3-wildtype and IDH-wildtype
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Disease
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| Infant-type hemispheric glioma
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Disease
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| Pilocytic astrocytoma
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Disease
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| High-grade astrocytoma with piloid features
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Disease
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| Pleomorphic xanthoastrocytoma
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Disease
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| Subependymal giant cell astrocytoma
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Disease
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| Chordoid glioma
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Disease
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| Astroblastoma, MN1-altered
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Disease
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| Ganglioglioma
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Disease
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| Gangliocytoma
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Disease
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| Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma
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Disease
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| Dysembryoplastic neuroepithelial tumour
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Disease
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| Diffuse glioneuronal tumour with oligodendroglioma-like features and nuclear clusters
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Disease
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| Papillary glioneuronal tumour
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Disease
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| Rosette-forming glioneuronal tumour
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Disease
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| Myxoid glioneuronal tumour
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Disease
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| Diffuse leptomeningeal glioneuronal tumour
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Disease
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| Multinodular and vacuolating neuronal tumour
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Disease
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| Dysplastic cerebellar gangliocytoma (Lhermitte-Duclos disease)
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Disease
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| Central neurocytoma
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Disease
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| Extraventricular neurocytoma
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Disease
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| Cerebellar liponeurocytoma
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Disease
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| Supratentorial ependymoma
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Disease
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| Supratentorial ependymoma, ZFTA fusion-positive
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Disease
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| Supratentorial ependymoma, YAP1 fusion-positive
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Disease
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| Posterior fossa ependymoma
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Disease
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| Posterior fossa group A (PFA) ependymoma
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Disease
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| Posterior fossa group B (PFB) ependymoma
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Disease
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| Spinal ependymoma
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Disease
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| Spinal ependymoma, MYCN-amplified
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Disease
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| Myxopapillary ependymoma
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Disease
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| Subependymoma
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Disease
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| Choroid plexus papilloma
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Disease
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| Atypical choroid plexus papilloma
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Disease
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| Choroid plexus carcinoma
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Disease
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| Medulloblastoma, WNT-activated
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Disease
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| Medulloblastoma, SHH-activated and TP53-wildtype
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Disease
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| Medulloblastoma, SHH-activated and TP53-mutant
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Disease
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| Medulloblastoma, non-WNT/non-SHH
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Disease
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| Medulloblastoma, histologically defined
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Disease
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| Atypical teratoid/rhabdoid tumour
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Disease
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| Cribriform neuroepithelial tumour
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Disease
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| Embryonal tumour with multilayered rosettes
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Disease
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| CNS neuroblastoma, FOXR2-activated
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Disease
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| CNS tumour with BCOR internal tandem duplication
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Disease
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| CNS embryonal tumour NEC/NOS
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Disease
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| Pineocytoma
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Disease
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| Pineal parenchymal tumour of intermediate differentiation
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Disease
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| Pineoblastoma
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Disease
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| Papillary tumour of the pineal region
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Disease
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| Desmoplastic myxoid tumour of the pineal region, SMARCB1-mutant
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Disease
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| Schwannoma
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Disease
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| Neurofibroma
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Disease
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| Perineurioma
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Disease
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| Hybrid nerve sheath tumours
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Disease
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| Malignant melanotic nerve sheath tumour
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Disease
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| Malignant peripheral nerve sheath tumour
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Disease
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| Cauda equina neuroendocrine tumour (previously paraganglioma)
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Disease
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| Meningioma
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Disease
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| Solitary fibrous tumour
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Disease
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| Haemangiomas and vascular malformations
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Disease
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| Haemangioblastoma
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Disease
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| Rhabdomyosarcoma
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Disease
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| Intracranial mesenchymal tumour, FET::CREB fusion-positive
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Disease
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| CIC-rearranged sarcoma
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Disease
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| Primary intracranial sarcoma, DICER1-mutant
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Disease
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| Ewing sarcoma
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Disease
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| Mesenchymal chondrosarcoma
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Disease
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| Chondrosarcoma
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Disease
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| Chordoma
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Disease
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| Diffuse meningeal melanocytic neoplasms: Melanocytosis and melanomatosis
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Disease
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| Circumscribed meningeal melanocytic neoplasms: Melanocytoma and melanoma
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Disease
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| Primary diffuse large B-cell lymphoma of the CNS
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Disease
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| Immunodeficiency-associated CNS lymphomas
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Disease
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| Lymphomatoid granulomatosis
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Disease
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| Intravascular large B-cell lymphoma
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Disease
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| MALT lymphoma of the dura
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Disease
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| Other low-grade B-cell lymphomas of the CNS
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Disease
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| Anaplastic large cell lymphoma (ALK+/ALK−)
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Disease
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| T-cell and NK/T-cell lymphomas
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Disease
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| Erdheim-Chester disease
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Disease
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| Rosai-Dorfman disease
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Disease
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| Juvenile xanthogranuloma
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Disease
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| Langerhans cell histiocytosis
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Disease
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| Histiocytic sarcoma
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Disease
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| Germ cell tumours of the CNS
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Disease
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| Adamantinomatous craniopharyngioma
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Disease
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| Papillary craniopharyngioma
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Disease
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| Pituicytoma, granular cell tumour of the sellar region, and spindle cell oncocytoma
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Disease
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| Pituitary adenoma / pituitary neuroendocrine tumour
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Disease
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| Pituitary blastoma
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Disease
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| Metastases to the brain and spinal cord parenchyma
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Disease
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| Metastases to the meninges
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Disease
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| Neurofibromatosis type 1
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Disease
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| Neurofibromatosis type 2
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Disease
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| Schwannomatosis
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Disease
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| Von Hippel-Lindau syndrome
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Disease
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| Tuberous sclerosis
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Disease
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| Li-Fraumeni syndrome
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Disease
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| Cowden syndrome
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Disease
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| Constitutional mismatch repair deficiency syndrome
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Disease
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| Familial adenomatous polyposis 1
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Disease
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| Naevoid basal cell carcinoma syndrome
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Disease
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| Rhabdoid tumour predisposition syndrome
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Disease
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| Carney complex
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Disease
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| DICER1 syndrome
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Disease
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| Familial paraganglioma syndromes
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Disease
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| Melanoma-astrocytoma syndrome
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Disease
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| Familial retinoblastoma
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Disease
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| BAP1 tumour predisposition syndrome
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Disease
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| Fanconi anaemia
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Disease
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| ELP1-medulloblastoma syndrome
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Disease
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