HAN5:Volunteer Assignments and Opportunities: Difference between revisions

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!'''Notes'''
!'''Notes'''
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|[[GTS5:Hereditary_papillary_renal_carcinoma_(MET)|Hereditary papillary renal carcinoma (MET)]]
|CHAPTER 2 (NASAL, PARANASAL, AND SKULL BASE TUMOURS)
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|[[HAN5:Respiratory_epithelial_adenomatoid_hamartoma|Respiratory epithelial adenomatoid hamartoma]]
|Disease
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|[[HAN5:Seromucinous_hamartoma|Seromucinous hamartoma]]
|Disease
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|[[HAN5:Nasal_chondromesenchymal_hamartoma|Nasal chondromesenchymal hamartoma]]
|Disease
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|[[HAN5:Sinonasal_papilloma,_inverted_type|Sinonasal papilloma, inverted type]]
|Disease
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|[[HAN5:Sinonasal_papilloma,_oncocytic_type|Sinonasal papilloma, oncocytic type]]
|Disease
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|[[HAN5:Sinonasal_papilloma,_exophytic_type|Sinonasal papilloma, exophytic type]]
|Disease
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|-
|[[HAN5:Keratinizing_squamous_cell_carcinoma|Keratinizing squamous cell carcinoma]]
|Disease
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|-
|[[HAN5:Non-keratinizing_squamous_cell_carcinoma|Non-keratinizing squamous cell carcinoma]]
|Disease
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|[[HAN5:NUT_carcinoma|NUT carcinoma]]
|Disease
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|[[HAN5:SWI/SNF_complex-deficient_sinonasal_carcinoma|SWI/SNF complex-deficient sinonasal carcinoma]]
|Disease
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|[[HAN5:Sinonasal_lymphoepithelial_carcinoma|Sinonasal lymphoepithelial carcinoma]]
|Disease
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|[[HAN5:Sinonasal_undifferentiated_carcinoma|Sinonasal undifferentiated carcinoma]]
|Disease
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|[[HAN5:Teratocarcinosarcoma|Teratocarcinosarcoma]]
|Disease
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|[[HAN5:HPV-associated_multiphenotypic_sinonasal_carcinoma|HPV-associated multiphenotypic sinonasal carcinoma]]
|Disease
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|[[HAN5:Intestinal-type_sinonasal_adenocarcinoma|Intestinal-type sinonasal adenocarcinoma]]
|Disease
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|[[HAN5:Non-intestinal-type_sinonasal_adenocarcinoma|Non-intestinal-type sinonasal adenocarcinoma]]
|Disease
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|[[HAN5:Sinonasal_tract_angiofibroma_|Sinonasal tract angiofibroma]]
|Disease
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|[[HAN5:Sinonasal_glomangiopericytoma|Sinonasal glomangiopericytoma]]
|Disease
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|[[HAN5:Biphenotypic_sinonasal_sarcoma|Biphenotypic sinonasal sarcoma]]
|Disease
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|[[HAN5:Chordoma|Chordoma]]
|Disease
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|[[HAN5:Sinonasal_ameloblastoma|Sinonasal ameloblastoma]]
|Disease
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|[[HAN5:Adamantinomatous_craniopharyngioma|Adamantinomatous craniopharyngioma]]
|Disease
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|[[HAN5:Meningioma_of_the_sinonasal_tract,_ear,_and_temporal_bone|Meningioma of the sinonasal tract, ear, and temporal bone]]
|Disease
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|[[HAN5:Olfactory_neuroblastoma|Olfactory neuroblastoma]]
|Disease
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|[[HAN5:Hairy_polyp|Hairy polyp]]
|Disease
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|[[HAN5:Salivary_gland_anlage_tumour|Salivary gland anlage tumour]]
|Disease
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|[[HAN5:Low-grade_nasopharyngeal_papillary_adenocarcinoma|Low-grade nasopharyngeal papillary adenocarcinoma]]
|Disease
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|[[HAN5:Nasopharyngeal_carcinoma|Nasopharyngeal carcinoma]]
|Disease
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|[[HAN5:Squamous_papilloma_and_papillomatosis|Squamous papilloma and papillomatosis]]
|Disease
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|[[HAN5:Laryngeal_and_hypopharyngeal_epithelial_dysplasia|Laryngeal and hypopharyngeal epithelial dysplasia]]
|Disease
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|[[HAN5:Conventional_squamous_cell_carcinoma|Conventional squamous cell carcinoma]]
|Disease
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|[[HAN5:Verrucous_carcinoma_of_the_hypopharynx,_larynx,_trachea,_and_parapharyngeal_space|Verrucous carcinoma of the hypopharynx, larynx, trachea, and parapharyngeal space]]
|Disease
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|[[HAN5:Basaloid_squamous_cell_carcinoma|Basaloid squamous cell carcinoma]]
|Disease
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|[[HAN5:Papillary_squamous_cell_carcinoma|Papillary squamous cell carcinoma]]
|Disease
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|[[HAN5:Spindle_cell_squamous_carcinoma|Spindle cell squamous carcinoma]]
|Disease
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|[[HAN5:Adenosquamous_carcinoma|Adenosquamous carcinoma]]
|Disease
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|[[HAN5:Lymphoepithelial_carcinoma_of_the_larynx|Lymphoepithelial carcinoma of the larynx]]
|Disease
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|[[HAN5:Laryngeal_cartilaginous_tumours|Laryngeal cartilaginous tumours]]
|Disease
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|[[HAN5:Nodular_oncocytic_hyperplasia|Nodular oncocytic hyperplasia]]
|Disease
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|[[HAN5:Lymphoepithelial_sialadenitis|Lymphoepithelial sialadenitis]]
|Disease
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|[[HAN5:Pleomorphic_adenoma|Pleomorphic adenoma]]
|Disease
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|[[HAN5:Basal_cell_adenoma|Basal cell adenoma]]
|Disease
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|[[HAN5:Warthin_tumour|Warthin tumour]]
|Disease
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|[[HAN5:Oncocytoma|Oncocytoma]]
|Disease
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|[[HAN5:Salivary_gland_myoepithelioma|Salivary gland myoepithelioma]]
|Disease
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|[[HAN5:Canalicular_adenoma|Canalicular adenoma]]
|Disease
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|[[HAN5:Cystadenoma_of_the_salivary_glands|Cystadenoma of the salivary glands]]
|Disease
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|[[HAN5:Ductal_papillomas|Ductal papillomas]]
|Disease
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|[[HAN5:Sialadenoma_papilliferum|Sialadenoma papilliferum]]
|Disease
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|[[HAN5:Lymphadenoma_|Lymphadenoma]]
|Disease
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|[[HAN5:Sebaceous_adenoma_|Sebaceous adenoma]]
|Disease
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|[[HAN5:Intercalated_duct_adenoma_and_hyperplasia|Intercalated duct adenoma and hyperplasia]]
|Disease
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|[[HAN5:Striated_duct_adenoma|Striated duct adenoma]]
|Disease
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|[[HAN5:Sclerosing_polycystic_adenoma|Sclerosing polycystic adenoma]]
|Disease
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|[[HAN5:Keratocystoma|Keratocystoma]]
|Disease
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|[[HAN5:Mucoepidermoid_carcinoma|Mucoepidermoid carcinoma]]
|Disease
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|[[HAN5:Adenoid_cystic_carcinoma|Adenoid cystic carcinoma]]
|Disease
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|[[HAN5:Acinic_cell_carcinoma|Acinic cell carcinoma]]
|Disease
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|[[HAN5:Secretory_carcinoma|Secretory carcinoma]]
|Disease
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|[[HAN5:Microsecretory_adenocarcinoma|Microsecretory adenocarcinoma]]
|Disease
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|[[HAN5:Polymorphous_adenocarcinoma|Polymorphous adenocarcinoma]]
|Disease
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|[[HAN5:Hyalinizing_clear_cell_carcinoma|Hyalinizing clear cell carcinoma]]
|Disease
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|[[HAN5:Basal_cell_adenocarcinoma|Basal cell adenocarcinoma]]
|Disease
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|[[HAN5:Intraductal_carcinoma_|Intraductal carcinoma]]
|Disease
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|[[HAN5:Salivary_duct_carcinoma|Salivary duct carcinoma]]
|Disease
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|-
|[[HAN5:Myoepithelial_carcinoma|Myoepithelial carcinoma]]
|Disease
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|-
|[[HAN5:Epithelial-myoepithelial_carcinoma|Epithelial-myoepithelial carcinoma]]
|Disease
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|[[HAN5:Mucinous_adenocarcinoma|Mucinous adenocarcinoma]]
|Disease
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|[[HAN5:Sclerosing_microcystic_adenocarcinoma|Sclerosing microcystic adenocarcinoma]]
|Disease
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|[[HAN5:Carcinoma_ex_pleomorphic_adenoma|Carcinoma ex pleomorphic adenoma]]
|Disease
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|[[HAN5:Carcinosarcoma_of_the_salivary_glands|Carcinosarcoma of the salivary glands]]
|Disease
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|[[HAN5:Sebaceous_adenocarcinoma|Sebaceous adenocarcinoma]]
|Disease
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|[[HAN5:Lymphoepithelial_carcinoma|Lymphoepithelial carcinoma]]
|Disease
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|[[HAN5:Squamous_cell_carcinoma|Squamous cell carcinoma]]
|Disease
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|[[HAN5:Sialoblastoma|Sialoblastoma]]
|Disease
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|[[HAN5:Salivary_carcinoma_NOS_and_emerging_entities|Salivary carcinoma NOS and emerging entities]]
|Disease
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|[[HAN5:Sialolipoma|Sialolipoma]]
|Disease
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|[[HAN5:Necrotizing_sialometaplasia|Necrotizing sialometaplasia]]
|Disease
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|[[HAN5:Multifocal_epithelial_hyperplasia|Multifocal epithelial hyperplasia]]
|Disease
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|[[HAN5:Oral_melanoacanthoma|Oral melanoacanthoma]]
|Disease
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|[[HAN5:Squamous_papilloma|Squamous papilloma]]
|Disease
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|[[HAN5:Oral_potentially_malignant_disorders|Oral potentially malignant disorders]]
|Disease
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|[[HAN5:Oral_epithelial_dysplasia|Oral epithelial dysplasia]]
|Disease
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|[[HAN5:Proliferative_verrucous_leukoplakia|Proliferative verrucous leukoplakia]]
|Disease
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|[[HAN5:Submucous_fibrosis|Submucous fibrosis]]
|Disease
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|[[HAN5:HPV-associated_oral_epithelial_dysplasia|HPV-associated oral epithelial dysplasia]]
|Disease
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|-
|[[HAN5:Oral_squamous_cell_carcinoma|Oral squamous cell carcinoma]]
|Disease
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|-
|[[HAN5:Verrucous_carcinoma_of_the_oral_cavity_and_mobile_tongue|Verrucous carcinoma of the oral cavity and mobile tongue]]
|Disease
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|[[HAN5:Carcinoma_cuniculatum|Carcinoma cuniculatum]]
|Disease
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|[[HAN5:Congenital_granular_cell_epulis|Congenital granular cell epulis]]
|Disease
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|[[HAN5:Granular_cell_tumour|Granular cell tumour]]
|Disease
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|[[HAN5:Ectomesenchymal_chondromyxoid_tumour|Ectomesenchymal chondromyxoid tumour]]
|Disease
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|[[HAN5:Melanotic_neuroectodermal_tumour_of_infancy|Melanotic neuroectodermal tumour of infancy]]
|Disease
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|[[HAN5:Hamartomatous_polyps|Hamartomatous polyps]]
|Disease
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|[[HAN5:Squamous_cell_carcinoma,_HPV-associated|Squamous cell carcinoma, HPV-associated]]
|Disease
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|[[HAN5:Squamous_cell_carcinoma,_HPV-independent|Squamous cell carcinoma, HPV-independent]]
|Disease
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|[[HAN5:Radicular_cyst|Radicular cyst]]
|Disease
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|-
|[[HAN5:Inflammatory_collateral_cysts|Inflammatory collateral cysts]]
|Disease
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|[[HAN5:Surgical_ciliated_cyst|Surgical ciliated cyst]]
|Disease
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|[[HAN5:Nasopalatine_duct_cyst|Nasopalatine duct cyst]]
|Disease
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|-
|[[HAN5:Gingival_cysts|Gingival cysts]]
|Disease
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|-
|[[HAN5:Dentigerous_cyst|Dentigerous cyst]]
|Disease
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|[[HAN5:Orthokeratinized_odontogenic_cyst|Orthokeratinized odontogenic cyst]]
|Disease
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|-
|[[HAN5:Lateral_periodontal_cyst_and_botryoid_odontogenic_cyst|Lateral periodontal cyst and botryoid odontogenic cyst]]
|Disease
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|-
|[[HAN5:Calcifying_odontogenic_cyst|Calcifying odontogenic cyst]]
|Disease
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|-
|[[HAN5:Glandular_odontogenic_cyst|Glandular odontogenic cyst]]
|Disease
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|-
|[[HAN5:Odontogenic_keratocyst|Odontogenic keratocyst]]
|Disease
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|-
|[[HAN5:Adenomatoid_odontogenic_tumour|Adenomatoid odontogenic tumour]]
|Disease
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|-
|[[HAN5:Squamous_odontogenic_tumour|Squamous odontogenic tumour]]
|Disease
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|-
|[[HAN5:Calcifying_epithelial_odontogenic_tumour|Calcifying epithelial odontogenic tumour]]
|Disease
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|-
|[[HAN5:Ameloblastoma,_unicystic|Ameloblastoma, unicystic]]
|Disease
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|-
|[[HAN5:Ameloblastoma,_extraosseous/peripheral|Ameloblastoma, extraosseous/peripheral]]
|Disease
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|-
|[[HAN5:Ameloblastoma,_conventional|Ameloblastoma, conventional]]
|Disease
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|-
|[[HAN5:Adenoid_ameloblastoma|Adenoid ameloblastoma]]
|Disease
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|-
|[[HAN5:Metastasizing_ameloblastoma|Metastasizing ameloblastoma]]
|Disease
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|-
|[[HAN5:Odontoma|Odontoma]]
|Disease
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|[[HAN5:Primordial_odontogenic_tumour|Primordial odontogenic tumour]]
|Disease
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|-
|[[HAN5:Ameloblastic_fibroma|Ameloblastic fibroma]]
|Disease
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|-
|[[HAN5:Dentinogenic_ghost_cell_tumour|Dentinogenic ghost cell tumour]]
|Disease
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|-
|[[HAN5:Odontogenic_fibroma|Odontogenic fibroma]]
|Disease
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|-
|[[HAN5:Cementoblastoma|Cementoblastoma]]
|Disease
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|-
|[[HAN5:Cemento-ossifying_fibroma|Cemento-ossifying fibroma]]
|Disease
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|-
|[[HAN5:Odontogenic_myxoma|Odontogenic myxoma]]
|Disease
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|-
|[[HAN5:Sclerosing_odontogenic_carcinoma|Sclerosing odontogenic carcinoma]]
|Disease
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|-
|[[HAN5:Ameloblastic_carcinoma|Ameloblastic carcinoma]]
|Disease
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|-
|[[HAN5:Clear_cell_odontogenic_carcinoma|Clear cell odontogenic carcinoma]]
|Disease
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|-
|[[HAN5:Ghost_cell_odontogenic_carcinoma|Ghost cell odontogenic carcinoma]]
|Disease
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|-
|[[HAN5:Primary_intraosseous_carcinoma_NOS|Primary intraosseous carcinoma NOS]]
|Disease
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|-
|[[HAN5:Odontogenic_carcinosarcoma|Odontogenic carcinosarcoma]]
|Disease
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|-
|[[HAN5:Odontogenic_sarcomas|Odontogenic sarcomas]]
|Disease
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|[[HAN5:Central_giant_cell_granuloma|Central giant cell granuloma]]
|Disease
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|-
|[[HAN5:Peripheral_giant_cell_granuloma|Peripheral giant cell granuloma]]
|Disease
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|-
|[[HAN5:Cherubism|Cherubism]]
|Disease
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|-
|[[HAN5:Aneurysmal_bone_cyst|Aneurysmal bone cyst]]
|Disease
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|-
|[[HAN5:Simple_bone_cyst|Simple bone cyst]]
|Disease
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|-
|[[HAN5:Cemento-osseous_dysplasia|Cemento-osseous dysplasia]]
|Disease
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|-
|[[HAN5:Segmental_odontomaxillary_dysplasia|Segmental odontomaxillary dysplasia]]
|Disease
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|-
|[[HAN5:Fibrous_dysplasia|Fibrous dysplasia]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Juvenile_trabecular_ossifying_fibroma|Juvenile trabecular ossifying fibroma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Psammomatoid_ossifying_fibroma|Psammomatoid ossifying fibroma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Familial_gigantiform_cementoma|Familial gigantiform cementoma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Osteoma|Osteoma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Osteochondroma|Osteochondroma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Osteoblastoma|Osteoblastoma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Chondroblastoma|Chondroblastoma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Chondromyxoid_fibroma|Chondromyxoid fibroma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Desmoplastic_fibroma_of_bone|Desmoplastic fibroma of bone]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Osteosarcoma_of_the_jaw|Osteosarcoma of the jaw]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:The_chondrosarcoma_family_of_tumours|The chondrosarcoma family of tumours]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Mesenchymal_chondrosarcoma|Mesenchymal chondrosarcoma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Rhabdomyosarcoma_with_TFCP2_rearrangement_|Rhabdomyosarcoma with TFCP2 rearrangement]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Chondrodermatitis_nodularis_chronica_helicis|Chondrodermatitis nodularis chronica helicis]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Cystic_chondromalacia|Cystic chondromalacia]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Exostosis_(osteoma)_of_the_ear|Exostosis (osteoma) of the ear]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Ceruminous_adenoma|Ceruminous adenoma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Ceruminous_adenocarcinoma|Ceruminous adenocarcinoma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Squamous_cell_carcinoma_of_the_external_auditory_canal|Squamous cell carcinoma of the external auditory canal]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Otosclerosis|Otosclerosis]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Cholesteatoma|Cholesteatoma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Middle_ear_papilloma|Middle ear papilloma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Vestibular_schwannoma|Vestibular schwannoma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Middle_ear_neuroendocrine_tumour|Middle ear neuroendocrine tumour]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Endolymphatic_sac_tumour|Endolymphatic sac tumour]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Middle_ear_squamous_cell_carcinoma|Middle ear squamous cell carcinoma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Middle_ear_adenocarcinoma|Middle ear adenocarcinoma]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Lipomas|Lipomas]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Liposarcomas|Liposarcomas]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Nodular_fasciitis|Nodular fasciitis]]
|Disease
|
|
|
|
|
|
|
|
|-
|[[HAN5:Desmoid_fibromatosis|Desmoid fibromatosis]]
|Disease
|Disease
|
|
Line 28: Line 1,896:
|
|
|-
|-
|[[GTS5:Multiple_endocrine_neoplasia_type_2_(RET)|Multiple endocrine neoplasia type 2 (RET)]]
|[[HAN5:Solitary_fibrous_tumour|Solitary fibrous tumour]]
|Disease
|Disease
|
|
Line 39: Line 1,907:
|
|
|-
|-
|[[GTS5:Juvenile_polyposis_syndrome_(BMPR1A,_SMAD4)|Juvenile polyposis syndrome (BMPR1A, SMAD4)]]
|[[HAN5:Low-grade_myofibroblastic_sarcoma|Low-grade myofibroblastic sarcoma]]
|Disease
|Disease
|
|
Line 50: Line 1,918:
|
|
|-
|-
|[[GTS5:Hereditary_neuroblastoma_(ALK,_PHOX2B)|Hereditary neuroblastoma (ALK, PHOX2B)]]
|[[HAN5:Inflammatory_myofibroblastic_tumour|Inflammatory myofibroblastic tumour]]
|Disease
|Disease
|
|
Line 61: Line 1,929:
|
|
|-
|-
|[[GTS5:Encephalocraniocutaneous_lipomatosis_(FGFR1)|Encephalocraniocutaneous lipomatosis (FGFR1)]]
|[[HAN5:Haemangioma|Haemangioma]]
|Disease
|Disease
|
|
Line 72: Line 1,940:
|
|
|-
|-
|[[GTS5:Glucagon_cell_hyperplasia_and_neoplasia_(GCGR)|Glucagon cell hyperplasia and neoplasia (GCGR)]]
|[[HAN5:Epithelioid_haemangioma|Epithelioid haemangioma]]
|Disease
|Disease
|
|
Line 83: Line 1,951:
|
|
|-
|-
|[[GTS5:McCune-Albright_syndrome_(GNAS)|McCune-Albright syndrome (GNAS)]]
|[[HAN5:Lymphangioma|Lymphangioma]]
|Disease
|Disease
|
|
Line 94: Line 1,962:
|
|
|-
|-
|[[GTS5:Sturge-Weber_syndrome_(GNAQ)|Sturge-Weber syndrome (GNAQ)]]
|[[HAN5:Epithelioid_haemangioendothelioma|Epithelioid haemangioendothelioma]]
|Disease
|Disease
|
|
Line 105: Line 1,973:
|
|
|-
|-
|[[GTS5:Neurofibromatosis_type_1_(NF1)|Neurofibromatosis type 1 (NF1)]]
|[[HAN5:Kaposi_sarcoma|Kaposi sarcoma]]
|Disease
|Disease
|
|
Line 116: Line 1,984:
|
|
|-
|-
|[[GTS5:NF2-related_schwannomatosis_(NF2)|NF2-related schwannomatosis (NF2)]]
|[[HAN5:Angiosarcoma|Angiosarcoma]]
|Disease
|Disease
|
|
Line 127: Line 1,995:
|
|
|-
|-
|[[GTS5:Costello_syndrome_(HRAS)|Costello syndrome (HRAS)]]
|[[HAN5:Myofibroma|Myofibroma]]
|Disease
|Disease
|
|
Line 138: Line 2,006:
|
|
|-
|-
|[[GTS5:Noonan_syndrome_(Various_genes)|Noonan syndrome (Various genes)]]
|[[HAN5:Leiomyoma|Leiomyoma]]
|Disease
|Disease
|
|
Line 149: Line 2,017:
|
|
|-
|-
|[[GTS5:Schimmelpenning-Feuerstein-Mims_(HRAS,_KRAS)|Schimmelpenning-Feuerstein-Mims (HRAS, KRAS)]]
|[[HAN5:EBV-associated_smooth_muscle_tumour|EBV-associated smooth muscle tumour]]
|Disease
|Disease
|
|
Line 160: Line 2,028:
|
|
|-
|-
|[[GTS5:Carney_complex_(PRKAR1A,_PDE8B,_PDE11A)|Carney complex (PRKAR1A, PDE8B, PDE11A)]]
|[[HAN5:Smooth_muscle_tumour_of_uncertain_malignant_potential|Smooth muscle tumour of uncertain malignant potential]]
|Disease
|Disease
|
|
Line 171: Line 2,039:
|
|
|-
|-
|[[GTS5:PROS_syndrome_(PIK3CA)|PROS syndrome (PIK3CA)]]
|[[HAN5:Leiomyosarcoma|Leiomyosarcoma]]
|Disease
|Disease
|
|
Line 182: Line 2,050:
|
|
|-
|-
|[[GTS5:Familial_adenomatous_polyposis_(APC)|Familial adenomatous polyposis (APC)]]
|[[HAN5:Rhabdomyoma|Rhabdomyoma]]
|Disease
|Disease
|
|
Line 193: Line 2,061:
|
|
|-
|-
|[[GTS5:Gastric_Adenocarcinoma_and_Proximal_Polyposis_of_Stomach_-_GAPPS_(APC_promoter)|Gastric Adenocarcinoma and Proximal Polyposis of Stomach - GAPPS (APC promoter)]]
|[[HAN5:Rhabdomyosarcomas|Rhabdomyosarcomas]]
|Disease
|Disease
|
|
Line 204: Line 2,072:
|
|
|-
|-
|[[GTS5:AXIN2-associated_polyposis_(AXIN2)|AXIN2-associated polyposis (AXIN2)]]
|[[HAN5:Chondroma|Chondroma]]
|Disease
|Disease
|
|
Line 215: Line 2,083:
|
|
|-
|-
|[[GTS5:Serrated_polyposis_(RNF43)|Serrated polyposis (RNF43)]]
|[[HAN5:Neurofibroma|Neurofibroma]]
|Disease
|Disease
|
|
Line 226: Line 2,094:
|
|
|-
|-
|[[GTS5:WT1_related_tumour_predisposition_syndrome_(WT1)|WT1 related tumour predisposition syndrome (WT1)]]
|[[HAN5:Schwannoma|Schwannoma]]
|Disease
|Disease
|
|
Line 237: Line 2,105:
|
|
|-
|-
|[[GTS5:WAGR_syndrome_(WT1)|WAGR syndrome (WT1)]]
|[[HAN5:Neuromas_|Neuromas]]
|Disease
|Disease
|
|
Line 248: Line 2,116:
|
|
|-
|-
|[[GTS5:Multiple_endocrine_neoplasia_type_1_(MEN1)|Multiple endocrine neoplasia type 1 (MEN1)]]
|[[HAN5:Malignant_peripheral_nerve_sheath_tumour|Malignant peripheral nerve sheath tumour]]
|Disease
|Disease
|
|
Line 259: Line 2,127:
|
|
|-
|-
|[[GTS5:Peutz-Jeghers_syndrome_(STK11)|Peutz-Jeghers syndrome (STK11)]]
|[[HAN5:Phosphaturic_mesenchymal_tumour|Phosphaturic mesenchymal tumour]]
|Disease
|Disease
|
|
Line 270: Line 2,138:
|
|
|-
|-
|[[GTS5:Hereditary_gastric_and_breast_cancer_syndrome_(CDH1,_CTNNA1)|Hereditary gastric and breast cancer syndrome (CDH1, CTNNA1)]]
|[[HAN5:Myxoma_|Myxoma]]
|Disease
|Disease
|
|
Line 281: Line 2,149:
|
|
|-
|-
|[[GTS5:Hereditary_mixed_polyposis_syndrome_(GREM1)|Hereditary mixed polyposis syndrome (GREM1)]]
|[[HAN5:Extraskeletal_myxoid_chondrosarcoma|Extraskeletal myxoid chondrosarcoma]]
|Disease
|Disease
|
|
Line 292: Line 2,160:
|
|
|-
|-
|[[GTS5:Naevoid_basal_cell_carcinoma_syndrome_-_Gorlin_syndrome_(PTCH1,_SUFU,_GPR161)|Naevoid basal cell carcinoma syndrome - Gorlin syndrome (PTCH1, SUFU, GPR161)]]
|[[HAN5:Synovial_sarcoma|Synovial sarcoma]]
|Disease
|Disease
|
|
Line 303: Line 2,171:
|
|
|-
|-
|[[GTS5:SMO-related_Curry-Jones_syndrome_(SMO)|SMO-related Curry-Jones syndrome (SMO)]]
|[[HAN5:GLI1-altered_soft_tissue_tumour_|GLI1-altered soft tissue tumour]]
|Disease
|Disease
|
|
Line 314: Line 2,182:
|
|
|-
|-
|[[GTS5:ELP1-related_medulloblastoma_predisposition_syndrome(ELP1)|ELP1-related medulloblastoma predisposition syndrome(ELP1)]]
|[[HAN5:Undifferentiated_sarcoma|Undifferentiated sarcoma]]
|Disease
|Disease
|
|
Line 325: Line 2,193:
|
|
|-
|-
|[[GTS5:Osteochondromatosis_(EXT1,_EXT2)|Osteochondromatosis (EXT1, EXT2)]]
|[[HAN5:Ewing_sarcoma|Ewing sarcoma]]
|Disease
|Disease
|
|
Line 336: Line 2,204:
|
|
|-
|-
|[[GTS5:Brooke-Spiegler_syndrome_(CYLD)|Brooke-Spiegler syndrome (CYLD)]]
|[[HAN5:Reactive_lymphoid_hyperplasia|Reactive lymphoid hyperplasia]]
|Disease
|Disease
|
|
Line 347: Line 2,215:
|
|
|-
|-
|[[GTS5:Tuberous_sclerosis_(TSC1,_TSC1)|Tuberous sclerosis (TSC1, TSC1)]]
|[[HAN5:EBV-positive_mucocutaneous_ulcer|EBV-positive mucocutaneous ulcer]]
|Disease
|Disease
|
|
Line 358: Line 2,226:
|
|
|-
|-
|[[GTS5:PTEN_hamartoma_tumour_syndrome_(PTEN)|PTEN hamartoma tumour syndrome (PTEN)]]
|[[HAN5:IgG4-related_disease|IgG4-related disease]]
|Disease
|Disease
|
|
Line 369: Line 2,237:
|
|
|-
|-
|[[GTS5:Activated_Phosphatidylinositol-3-OH_kinase_δ_Syndrome_-_APDS_(PIK3CD)|Activated Phosphatidylinositol-3-OH kinase δ Syndrome - APDS (PIK3CD)]]
|[[HAN5:Extramedullary_myeloid_sarcoma|Extramedullary myeloid sarcoma]]
|Disease
|Disease
|
|
Line 380: Line 2,248:
|
|
|-
|-
|[[GTS5:Multiple_endocrine_neoplasia_type_5,_MAX_related_tumours_(MAX)|Multiple endocrine neoplasia type 5, MAX related tumours (MAX)]]
|[[HAN5:Extranodal_marginal_zone_lymphoma_of_mucosa-associated_lymphoid_tissue_(MALT_lymphoma)|Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma)]]
|Disease
|Disease
|
|
Line 391: Line 2,259:
|
|
|-
|-
|[[GTS5:MAFA-related_familial_insulinomatosis_(MAFA)|MAFA-related familial insulinomatosis (MAFA)]]
|[[HAN5:Mantle_cell_lymphoma|Mantle cell lymphoma]]
|Disease
|Disease
|
|
Line 402: Line 2,270:
|
|
|-
|-
|[[GTS5:Birt-Hogg-Dube_syndrome_(FLCN)|Birt-Hogg-Dube syndrome (FLCN)]]
|[[HAN5:Follicular_lymphoma|Follicular lymphoma]]
|Disease
|Disease
|
|
Line 413: Line 2,281:
|
|
|-
|-
|[[GTS5:Familial_chordoma_(TBXT)|Familial chordoma (TBXT)]]
|[[HAN5:Paediatric-type_follicular_lymphoma|Paediatric-type follicular lymphoma]]
|Disease
|Disease
|
|
Line 424: Line 2,292:
|
|
|-
|-
|[[GTS5:Hyperparathyroidism_jaw_tumour_syndrome_(CDC73)|Hyperparathyroidism jaw tumour syndrome (CDC73)]]
|[[HAN5:Large_B-cell_lymphoma_with_IRF4_rearrangement|Large B-cell lymphoma with IRF4 rearrangement]]
|Disease
|Disease
|
|
Line 435: Line 2,303:
|
|
|-
|-
|[[GTS5:Von_Hippel-Lindau_syndrome_(VHL)|Von Hippel-Lindau syndrome (VHL)]]
|[[HAN5:Diffuse_large_B-cell_lymphoma|Diffuse large B-cell lymphoma]]
|Disease
|Disease
|
|
Line 446: Line 2,314:
|
|
|-
|-
|[[GTS5:SDH-deficient_tumour_syndrome_-_Hereditary_phaeochromocytoma-paraganglioma_syndromes_(SDHA,_SDHB,_SDHC,_SDHD,_SDHAF2)|SDH-deficient tumour syndrome - Hereditary phaeochromocytoma-paraganglioma syndromes (SDHA, SDHB, SDHC, SDHD, SDHAF2)]]
|[[HAN5:Burkitt_lymphoma|Burkitt lymphoma]]
|Disease
|Disease
|
|
Line 457: Line 2,325:
|
|
|-
|-
|[[GTS5:Hereditary_leiomyomatosis_and_renal_cell_carcinoma_syndrome_(FH)|Hereditary leiomyomatosis and renal cell carcinoma syndrome (FH)]]
|[[HAN5:Plasmacytoma|Plasmacytoma]]
|Disease
|Disease
|
|
Line 468: Line 2,336:
|
|
|-
|-
|[[GTS5:Hereditary_tyrosinaemia_type_1_(FAH)|Hereditary tyrosinaemia type 1 (FAH)]]
|[[HAN5:Plasmablastic_lymphoma|Plasmablastic lymphoma]]
|Disease
|Disease
|
|
Line 479: Line 2,347:
|
|
|-
|-
|[[GTS5:Li-Fraumeni_syndrome_(TP53)|Li-Fraumeni syndrome (TP53)]]
|[[HAN5:T-lymphoblastic_leukaemia/lymphoma|T-lymphoblastic leukaemia/lymphoma]]
|Disease
|Disease
|
|
Line 490: Line 2,358:
|
|
|-
|-
|[[GTS5:Retinoblastoma_syndrome_(RB1)|Retinoblastoma syndrome (RB1)]]
|[[HAN5:Primary_mucosal_CD30-positive_T-cell_lymphoproliferative_disorder|Primary mucosal CD30-positive T-cell lymphoproliferative disorder]]
|Disease
|Disease
|
|
Line 501: Line 2,369:
|
|
|-
|-
|[[GTS5:Multiple_endocrine_neoplasia_type_4_(CDKN1B)|Multiple endocrine neoplasia type 4 (CDKN1B)]]
|[[HAN5:Extranodal_NK/T-cell_lymphoma|Extranodal NK/T-cell lymphoma]]
|Disease
|Disease
|
|
Line 512: Line 2,380:
|
|
|-
|-
|[[GTS5:CDKN2A-related_tumour_predisposition_syndrome_(CDKN2A)|CDKN2A-related tumour predisposition syndrome (CDKN2A)]]
|[[HAN5:Hodgkin_lymphoma|Hodgkin lymphoma]]
|Disease
|Disease
|
|
Line 523: Line 2,391:
|
|
|-
|-
|[[GTS5:CDK4-related_melanoma_predisposition_syndrome_(CDK4)|CDK4-related melanoma predisposition syndrome (CDK4)]]
|[[HAN5:Juvenile_xanthogranuloma|Juvenile xanthogranuloma]]
|Disease
|Disease
|
|
Line 534: Line 2,402:
|
|
|-
|-
|[[GTS5:Autoimmune_lymphoproliferative_syndrome_(FAS)|Autoimmune lymphoproliferative syndrome (FAS)]]
|[[HAN5:Erdheim-Chester_disease|Erdheim-Chester disease]]
|Disease
|Disease
|
|
Line 545: Line 2,413:
|
|
|-
|-
|[[GTS5:Lynch_Syndrome_(MLH1,_PMS2,_MSH2,_MSH6)|Lynch Syndrome (MLH1, PMS2, MSH2, MSH6)]]
|[[HAN5:Rosai-Dorfman_disease|Rosai-Dorfman disease]]
|Disease
|Disease
|
|
Line 556: Line 2,424:
|
|
|-
|-
|[[GTS5:Muir-Torre_syndrome_(MLH1,_PMS2,_MSH2,_MSH6)|Muir-Torre syndrome (MLH1, PMS2, MSH2, MSH6)]]
|[[HAN5:Langerhans_cell_histiocytosis|Langerhans cell histiocytosis]]
|Disease
|Disease
|
|
Line 567: Line 2,435:
|
|
|-
|-
|[[GTS5:Constitutional_mismatch_repair_deficiency_(CMMRD)_syndrome_(MLH1,_PMS2,_MSH2,_MSH6)|Constitutional mismatch repair deficiency (CMMRD) syndrome (MLH1, PMS2, MSH2, MSH6)]]
|[[HAN5:Follicular_dendritic_cell_sarcoma|Follicular dendritic cell sarcoma]]
|Disease
|Disease
|
|
Line 578: Line 2,446:
|
|
|-
|-
|[[GTS5:BRCA-related_cancer_predisposition_syndrome_(BRCA1,_BRCA2)|BRCA-related cancer predisposition syndrome (BRCA1, BRCA2)]]
|[[HAN5:Mucosal_melanoma|Mucosal melanoma]]
|Disease
|Disease
|
|
Line 589: Line 2,457:
|
|
|-
|-
|[[GTS5:PALB2-related_cancer_predisposition_syndrome_(PALB2)|PALB2-related cancer predisposition syndrome (PALB2)]]
|[[HAN5:Ranula|Ranula]]
|Disease
|Disease
|
|
Line 600: Line 2,468:
|
|
|-
|-
|[[GTS5:RAD51-related_cancer_predisposition_syndrome_(RAD51C,_RAD51D)|RAD51-related cancer predisposition syndrome (RAD51C, RAD51D)]]
|[[HAN5:Lymphoepithelial_cyst|Lymphoepithelial cyst]]
|Disease
|Disease
|
|
Line 611: Line 2,479:
|
|
|-
|-
|[[GTS5:Fanconi_anaemia_(FANC_genes)|Fanconi anaemia (FANC genes)]]
|[[HAN5:Branchial_cleft_cyst|Branchial cleft cyst]]
|Disease
|Disease
|
|
Line 622: Line 2,490:
|
|
|-
|-
|[[GTS5:MUTYH-associated_polyposis_(MUTYH)|MUTYH-associated polyposis (MUTYH)]]
|[[HAN5:Thyroglossal_duct_cyst|Thyroglossal duct cyst]]
|Disease
|Disease
|
|
Line 633: Line 2,501:
|
|
|-
|-
|[[GTS5:NTHL1-related_tumour_syndrome_(NTHL1)|NTHL1-related tumour syndrome (NTHL1)]]
|[[HAN5:Dermoid_and_teratoid_cysts|Dermoid and teratoid cysts]]
|Disease
|Disease
|
|
Line 644: Line 2,512:
|
|
|-
|-
|[[GTS5:MBD4-associated_neoplasia_syndrome_(MBD4)|MBD4-associated neoplasia syndrome (MBD4)]]
|[[HAN5:Branchioma|Branchioma]]
|Disease
|Disease
|
|
Line 655: Line 2,523:
|
|
|-
|-
|[[GTS5:Xeroderma_Pigmentosum|Xeroderma Pigmentosum]]
|[[HAN5:Heterotopia-associated_carcinoma|Heterotopia-associated carcinoma]]
|Disease
|Disease
|
|
Line 666: Line 2,534:
|
|
|-
|-
|[[GTS5:Ataxia-telangiectasia_syndrome_(ATM)|Ataxia-telangiectasia syndrome (ATM)]]
|[[HAN5:Squamous_carcinoma_of_unknown_primary_site|Squamous carcinoma of unknown primary site]]
|Disease
|Disease
|
|
Line 677: Line 2,545:
|
|
|-
|-
|[[GTS5:CHEK2-related_hereditary_(breast)_cancer_predisposition_syndrome_(CHEK2)|CHEK2-related hereditary (breast) cancer predisposition syndrome (CHEK2)]]
|[[HAN5:Germ_cell_tumours_of_the_head_and_neck|Germ cell tumours of the head and neck]]
|Disease
|Disease
|
|
Line 688: Line 2,556:
|
|
|-
|-
|[[GTS5:Nijmegen_breakage_syndrome_(NBN)|Nijmegen breakage syndrome (NBN)]]
|[[HAN5:Metastases_to_the_head_and_neck_region|Metastases to the head and neck region]]
|Disease
|Disease
|
|
Line 699: Line 2,567:
|
|
|-
|-
|[[GTS5:Polymerase_proofreading-associated_polyposis_(POLD1,_POLE)|Polymerase proofreading-associated polyposis (POLD1, POLE)]]
|[[HAN5:Neuroendocrine_tumour|Neuroendocrine tumour]]
|Disease
|Disease
|
|
Line 710: Line 2,578:
|
|
|-
|-
|[[GTS5:Bloom_syndrome_(BLM)|Bloom syndrome (BLM)]]
|[[HAN5:Ectopic_or_invasive_PitNET_/_pituitary_adenoma|Ectopic or invasive PitNET / pituitary adenoma]]
|Disease
|Disease
|
|
Line 721: Line 2,589:
|
|
|-
|-
|[[GTS5:Werner_syndrome_(WRN)|Werner syndrome (WRN)]]
|[[HAN5:Small_cell_neuroendocrine_carcinoma|Small cell neuroendocrine carcinoma]]
|Disease
|Disease
|
|
Line 732: Line 2,600:
|
|
|-
|-
|[[GTS5:Rothmund-Thomson_syndrome_(ANAPC1,_RECQL4)|Rothmund-Thomson syndrome (ANAPC1, RECQL4)]]
|[[HAN5:Large_cell_neuroendocrine_carcinoma|Large cell neuroendocrine carcinoma]]
|Disease
|Disease
|
|
Line 743: Line 2,611:
|
|
|-
|-
|[[GTS5:DDX41-related_haematologic_tumour_predisposition_syndrome_(DDX41)|DDX41-related haematologic tumour predisposition syndrome (DDX41)]]
|[[HAN5:Merkel_cell_carcinoma|Merkel cell carcinoma]]
|Disease
|Disease
|
|
Line 754: Line 2,622:
|
|
|-
|-
|[[GTS5:Mosaic_variegated_aneuploidy_(BUB1B,_CEP57,_TRIP13,_BUB1,_BUB3)|Mosaic variegated aneuploidy (BUB1B, CEP57, TRIP13, BUB1, BUB3)]]
|[[HAN5:Head_and_neck_paraganglioma|Head and neck paraganglioma]]
|Disease
|Disease
|
|
Line 765: Line 2,633:
|
|
|-
|-
|[[GTS5:Klinefelter_syndrome|Klinefelter syndrome]]
|[[HAN5:Naevoid_basal_cell_carcinoma_syndrome_(Gorlin_syndrome)|Naevoid basal cell carcinoma syndrome (Gorlin syndrome)]]
|Disease
|Disease
|
|
Line 776: Line 2,644:
|
|
|-
|-
|[[GTS5:Turner_syndrome|Turner syndrome]]
|[[HAN5:Neurofibromatosis_type_1|Neurofibromatosis type 1]]
|Disease
|Disease
|
|
Line 787: Line 2,655:
|
|
|-
|-
|[[GTS5:Down_syndrome|Down syndrome]]
|[[HAN5:Familial_adenomatous_polyposis_and_Gardner_syndrome|Familial adenomatous polyposis and Gardner syndrome]]
|Disease
|Disease
|
|
Line 798: Line 2,666:
|
|
|-
|-
|[[GTS5:Dyskeratosis_congenita_(DKC1,_TERT,_TERC,_TINF2,_Other_IBMFS_genes)|Dyskeratosis congenita (DKC1, TERT, TERC, TINF2, Other IBMFS genes)]]
|[[HAN5:Brooke-Spiegler_syndrome|Brooke-Spiegler syndrome]]
|Disease
|Disease
|
|
Line 809: Line 2,677:
|
|
|-
|-
|[[GTS5:POT1_and_Shelterin-related_tumour_predisposition_syndrome_(POT1,_ACD,_TERF2IP,_TERT_promoter)|POT1 and Shelterin-related tumour predisposition syndrome (POT1, ACD, TERF2IP, TERT promoter)]]
|[[HAN5:Cowden_syndrome|Cowden syndrome]]
|Disease
|Disease
|
|
Line 820: Line 2,688:
|
|
|-
|-
|[[GTS5:Beckwith-Wiedemann_spectrum_(IGF2;_CDKN1C)|Beckwith-Wiedemann spectrum (IGF2; CDKN1C)]]
|[[HAN5:Familial_paraganglioma_syndromes|Familial paraganglioma syndromes]]
|Disease
|Disease
|
|
Line 831: Line 2,699:
|
|
|-
|-
|[[GTS5:Enchondromatosis_(IDH1,_IDH2)|Enchondromatosis (IDH1, IDH2)]]
|[[HAN5:Multiple_endocrine_neoplasia_type_2|Multiple endocrine neoplasia type 2]]
|Disease
|Disease
|
|
Line 842: Line 2,710:
|
|
|-
|-
|[[GTS5:Rhabdoid_tumour_predisposition_syndrome_(SMARCB1,_SMARCA4)|Rhabdoid tumour predisposition syndrome (SMARCB1, SMARCA4)]]
|[[HAN5:Hyperparathyroidism-jaw_tumour_syndrome|Hyperparathyroidism-jaw tumour syndrome]]
|Disease
|Disease
|
|
Line 853: Line 2,721:
|
|
|-
|-
|[[GTS5:Schwannomatosis_(SMARCB1,_LZTR1)|Schwannomatosis (SMARCB1, LZTR1)]]
|[[HAN5:Li-Fraumeni_syndrome|Li-Fraumeni syndrome]]
|Disease
|Disease
|
|
Line 864: Line 2,732:
|
|
|-
|-
|[[GTS5:Clear_cell_meningioma_predisposition_syndrome_(SMARCE1)|Clear cell meningioma predisposition syndrome (SMARCE1)]]
|[[HAN5:Fanconi_anaemia|Fanconi anaemia]]
|Disease
|Disease
|
|
Line 875: Line 2,743:
|
|
|-
|-
|[[GTS5:Weaver_syndrome_(EZH2)|Weaver syndrome (EZH2)]]
|[[HAN5:Dyskeratosis_congenita|Dyskeratosis congenita]]
|Disease
|Disease
|
|
Line 886: Line 2,754:
|
|
|-
|-
|[[GTS5:DICER1-related_tumour_predisposition_syndrome_(DICER1)|DICER1-related tumour predisposition syndrome (DICER1)]]
|[[HAN5:Ataxia-telangiectasia|Ataxia-telangiectasia]]
|Disease
|Disease
|
|
Line 897: Line 2,765:
|
|
|-
|-
|[[GTS5:MicroRNA_processor_tumour_predisposition_syndromes_(DROSHA,_DGCR8)|MicroRNA processor tumour predisposition syndromes (DROSHA, DGCR8)]]
|[[HAN5:Bloom_syndrome|Bloom syndrome]]
|Disease
|Disease
|
|
Line 908: Line 2,776:
|
|
|-
|-
|[[GTS5:Goldenhar_syndrome_(MYT1,_SF3B2)|Goldenhar syndrome (MYT1, SF3B2)]]
|[[HAN5:Von_Hippel-Lindau_syndrome|Von Hippel-Lindau syndrome]]
|Disease
|Disease
|
|
Line 919: Line 2,787:
|
|
|-
|-
|[[GTS5:BAP1-related_tumour_predisposition_syndrome_(BAP1)|BAP1-related tumour predisposition syndrome (BAP1)]]
|[[HAN5:Tuberous_sclerosis|Tuberous sclerosis]]
|Disease
|Disease
|
|