AlexanderDiseaseSjogren-LarssonSyndromeHereditary DiffuseLeukoencephalopathywith Spheroids (HDLS)Nasu-Hakola Disease(NHD) or PolycysticLipomembranousOsteodysplasia withSclerosingLeukoencephalopathy(PLOSL)Aicardi-GoutieresSyndromeAdultPolyglucosanBodyDiseaseFukuyamaCongenitalMuscularDystrophyGloboid CellLeukodystrophy(KrabbeDisease)PelizaeusMerzbacherDiseaseCanavanDiseaseRNAse T2-deficientLeukoencephalopathyGM1GangliosidosisAcuteHemorrhagicLeukoencephalitis(AHLE)Fatty AcidHydroxylase-AssociatedNeurodegeneration(FAHN)Hypomyelinationwith Atrophy ofthe BasalGanglia andCerebellum (H-ABC)Cerebral AutosomalDominant Arteriopathywith SubcorticalInfarcts andLeukoencephalopathy(CADASIL)VanishingWhite MatterDisease(VWM)Acute DisseminatedEncephalomyeolitis(ADEM)NeonatalAdrenoleukodystrophy(NALD)ZellwegerSyndromeCoats PlusSyndrome orCerebroretinalMicroangiographywith Calcificationsand Cysts(CRMCC)MetachromaticLeukodystrophy(MLD)RefsumDiseaseAdrenoleukodystrophy(ALD)GM2Gangliosidosis(Tay-SachsDisease)Adrenomyeloneuropathy(AMN)GalactosialidosisFucosidosisCerebrotendinousXanthomatosis(CTX)OculodentodigitalDysplasia withCerebral WhiteMatterAbnormalities(ODDD)InfantileRefsumDisease18qSyndromeAdult OnsetAutosomalDominantLeukodystrophy(ADLD)HypomyelinationwithHypogonadotropicHypogonadismand Hypodontia(4H Syndrome)Leukoencephalopathywith Brain Stem andSpinal CordInvolvement andLactate Elevation(LBSL)MegalencephalicLeukodystrophywith subcorticalCysts (MLC)AlexanderDiseaseSjogren-LarssonSyndromeHereditary DiffuseLeukoencephalopathywith Spheroids (HDLS)Nasu-Hakola Disease(NHD) or PolycysticLipomembranousOsteodysplasia withSclerosingLeukoencephalopathy(PLOSL)Aicardi-GoutieresSyndromeAdultPolyglucosanBodyDiseaseFukuyamaCongenitalMuscularDystrophyGloboid CellLeukodystrophy(KrabbeDisease)PelizaeusMerzbacherDiseaseCanavanDiseaseRNAse T2-deficientLeukoencephalopathyGM1GangliosidosisAcuteHemorrhagicLeukoencephalitis(AHLE)Fatty AcidHydroxylase-AssociatedNeurodegeneration(FAHN)Hypomyelinationwith Atrophy ofthe BasalGanglia andCerebellum (H-ABC)Cerebral AutosomalDominant Arteriopathywith SubcorticalInfarcts andLeukoencephalopathy(CADASIL)VanishingWhite MatterDisease(VWM)Acute DisseminatedEncephalomyeolitis(ADEM)NeonatalAdrenoleukodystrophy(NALD)ZellwegerSyndromeCoats PlusSyndrome orCerebroretinalMicroangiographywith Calcificationsand Cysts(CRMCC)MetachromaticLeukodystrophy(MLD)RefsumDiseaseAdrenoleukodystrophy(ALD)GM2Gangliosidosis(Tay-SachsDisease)Adrenomyeloneuropathy(AMN)GalactosialidosisFucosidosisCerebrotendinousXanthomatosis(CTX)OculodentodigitalDysplasia withCerebral WhiteMatterAbnormalities(ODDD)InfantileRefsumDisease18qSyndromeAdult OnsetAutosomalDominantLeukodystrophy(ADLD)HypomyelinationwithHypogonadotropicHypogonadismand Hypodontia(4H Syndrome)Leukoencephalopathywith Brain Stem andSpinal CordInvolvement andLactate Elevation(LBSL)MegalencephalicLeukodystrophywith subcorticalCysts (MLC)

Untitled Bingo - Call List

(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.


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  1. Alexander Disease
  2. Sjogren-Larsson Syndrome
  3. Hereditary Diffuse Leukoencephalopathy with Spheroids (HDLS)
  4. Nasu-Hakola Disease (NHD) or Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy (PLOSL)
  5. Aicardi-Goutieres Syndrome
  6. Adult Polyglucosan Body Disease
  7. Fukuyama Congenital Muscular Dystrophy
  8. Globoid Cell Leukodystrophy (Krabbe Disease)
  9. Pelizaeus Merzbacher Disease
  10. Canavan Disease
  11. RNAse T2-deficient Leukoencephalopathy
  12. GM1 Gangliosidosis
  13. Acute Hemorrhagic Leukoencephalitis (AHLE)
  14. Fatty Acid Hydroxylase-Associated Neurodegeneration (FAHN)
  15. Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum (H-ABC)
  16. Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)
  17. Vanishing White Matter Disease (VWM)
  18. Acute Disseminated Encephalomyeolitis (ADEM)
  19. Neonatal Adrenoleukodystrophy (NALD)
  20. Zellweger Syndrome
  21. Coats Plus Syndrome or Cerebroretinal Microangiography with Calcifications and Cysts (CRMCC)
  22. Metachromatic Leukodystrophy (MLD)
  23. Refsum Disease
  24. Adrenoleukodystrophy (ALD)
  25. GM2 Gangliosidosis (Tay-Sachs Disease)
  26. Adrenomyeloneuropathy (AMN)
  27. Galactosialidosis
  28. Fucosidosis
  29. Cerebrotendinous Xanthomatosis (CTX)
  30. Oculodentodigital Dysplasia with Cerebral White Matter Abnormalities (ODDD)
  31. Infantile Refsum Disease
  32. 18q Syndrome
  33. Adult Onset Autosomal Dominant Leukodystrophy (ADLD)
  34. Hypomyelination with Hypogonadotropic Hypogonadism and Hypodontia (4H Syndrome)
  35. Leukoencephalopathy with Brain Stem and Spinal Cord Involvement and Lactate Elevation (LBSL)
  36. Megalencephalic Leukodystrophy with subcortical Cysts (MLC)