Volunteer Assignments and Opportunities: Difference between revisions

{| class="wikitable"

|-

| Astrocytoma, IDH-mutant||Disease||

| Oligodendroglioma, IDH-mutant and 1p/19q-codeleted||Disease||

| Glioblastoma, IDH-wildtype||Disease||

| Diffuse astrocytoma, MYB- or MYBL1-altered||Disease||

| Angiocentric glioma||Disease||

| Polymorphous low-grade neuroepithelial tumour of the young||Disease||

| Diffuse low-grade glioma, MAPK pathway-altered ||Disease||

| Diffuse midline glioma, H3 K27-altered||Disease||

| Diffuse hemispheric glioma, H3 G34-mutant||Disease||

| Diffuse paediatric-type high-grade glioma, H3-wildtype and IDH-wildtype||Disease||

| Infant-type hemispheric glioma||Disease||

| Pilocytic astrocytoma ||Disease||

| High-grade astrocytoma with piloid features||Disease||

| Pleomorphic xanthoastrocytoma||Disease||

| Subependymal giant cell astrocytoma||Disease||

| Chordoid glioma||Disease||

| Astroblastoma, MN1-altered||Disease||

| Ganglioglioma||Disease||

| Gangliocytoma||Disease||

| Desmoplastic infantile ganglioglioma / desmoplastic infantile astrocytoma||Disease||

| Dysembryoplastic neuroepithelial tumour||Disease||

| Diffuse glioneuronal tumour with oligodendroglioma-like features and nuclear clusters||Disease||

| Papillary glioneuronal tumour||Disease||

| Rosette-forming glioneuronal tumour||Disease||

| Myxoid glioneuronal tumour||Disease||

| Diffuse leptomeningeal glioneuronal tumour||Disease||

| Multinodular and vacuolating neuronal tumour||Disease||

| Dysplastic cerebellar gangliocytoma (Lhermitte-Duclos disease)||Disease||

| Central neurocytoma||Disease||

| Extraventricular neurocytoma||Disease||

| Cerebellar liponeurocytoma||Disease||

| Supratentorial ependymoma||Disease||

| Supratentorial ependymoma, ZFTA fusion-positive ||Disease||

| Supratentorial ependymoma, YAP1 fusion-positive||Disease||

| Posterior fossa ependymoma||Disease||

| Posterior fossa group A (PFA) ependymoma||Disease||

| Posterior fossa group B (PFB) ependymoma||Disease||

| Spinal ependymoma||Disease||

| Spinal ependymoma, MYCN-amplified||Disease||

| Myxopapillary ependymoma||Disease||

| Subependymoma||Disease||

| Choroid plexus papilloma||Disease||

| Atypical choroid plexus papilloma||Disease||

| Choroid plexus carcinoma||Disease||

| Medulloblastoma, WNT-activated||Disease||

| Medulloblastoma, SHH-activated and TP53-wildtype||Disease||

| Medulloblastoma, SHH-activated and TP53-mutant||Disease||

| Medulloblastoma, non-WNT/non-SHH||Disease||

| Medulloblastoma, histologically defined||Disease||

| Atypical teratoid/rhabdoid tumour||Disease||

| Cribriform neuroepithelial tumour||Disease||

| Embryonal tumour with multilayered rosettes||Disease||

| CNS neuroblastoma, FOXR2-activated||Disease||

| CNS tumour with BCOR internal tandem duplication||Disease||

| CNS embryonal tumour NEC/NOS||Disease||

| Pineocytoma||Disease||

| Pineal parenchymal tumour of intermediate differentiation||Disease||

| Pineoblastoma||Disease||

| Papillary tumour of the pineal region||Disease||

| Desmoplastic myxoid tumour of the pineal region, SMARCB1-mutant||Disease||

| Schwannoma||Disease||

| Neurofibroma||Disease||

| Perineurioma||Disease||

| Hybrid nerve sheath tumours||Disease||

| Malignant melanotic nerve sheath tumour||Disease||

| Malignant peripheral nerve sheath tumour||Disease||

| Cauda equina neuroendocrine tumour (previously paraganglioma)||Disease||

| Meningioma||Disease||

| Solitary fibrous tumour||Disease||

| Haemangiomas and vascular malformations||Disease||

| Haemangioblastoma||Disease||

| Rhabdomyosarcoma||Disease||

| Intracranial mesenchymal tumour, FET::CREB fusion-positive||Disease||

| CIC-rearranged sarcoma||Disease||

| Primary intracranial sarcoma, DICER1-mutant||Disease||

| Ewing sarcoma||Disease||

| Mesenchymal chondrosarcoma||Disease||

| Chondrosarcoma||Disease||

| Chordoma||Disease||

| Diffuse meningeal melanocytic neoplasms: Melanocytosis and melanomatosis||Disease||

| Circumscribed meningeal melanocytic neoplasms: Melanocytoma and melanoma||Disease||

| Primary diffuse large B-cell lymphoma of the CNS||Disease||

| Immunodeficiency-associated CNS lymphomas||Disease||

| Lymphomatoid granulomatosis||Disease||

| Intravascular large B-cell lymphoma||Disease||

| MALT lymphoma of the dura||Disease||

| Other low-grade B-cell lymphomas of the CNS||Disease||

| Anaplastic large cell lymphoma (ALK+/ALK−)||Disease||

| T-cell and NK/T-cell lymphomas||Disease||

| Erdheim-Chester disease||Disease||

| Rosai-Dorfman disease||Disease||

| Juvenile xanthogranuloma||Disease||

| Langerhans cell histiocytosis||Disease||

| Histiocytic sarcoma||Disease||

| Germ cell tumours of the CNS||Disease||

| Adamantinomatous craniopharyngioma||Disease||

| Papillary craniopharyngioma||Disease||

| Pituicytoma, granular cell tumour of the sellar region, and spindle cell oncocytoma||Disease||

| Pituitary adenoma / pituitary neuroendocrine tumour||Disease||

| Pituitary blastoma||Disease||

| Metastases to the brain and spinal cord parenchyma||Disease||

| Metastases to the meninges||Disease||

| Neurofibromatosis type 1||Disease||

| Neurofibromatosis type 2||Disease||

| Schwannomatosis||Disease||

| Von Hippel-Lindau syndrome||Disease||

| Tuberous sclerosis||Disease||

| Li-Fraumeni syndrome||Disease||

| Cowden syndrome||Disease||

| Constitutional mismatch repair deficiency syndrome||Disease||

| Familial adenomatous polyposis 1||Disease||

| Naevoid basal cell carcinoma syndrome||Disease||

| Rhabdoid tumour predisposition syndrome||Disease||

| Carney complex||Disease||

| DICER1 syndrome||Disease||

| Familial paraganglioma syndromes||Disease||

| Melanoma-astrocytoma syndrome||Disease||

| Familial retinoblastoma||Disease||

| BAP1 tumour predisposition syndrome||Disease||

| Fanconi anaemia||Disease||

| ELP1-medulloblastoma syndrome||Disease||