Nasu-Hakola Disease(NHD) or PolycysticLipomembranousOsteodysplasia withSclerosingLeukoencephalopathy(PLOSL)NeonatalAdrenoleukodystrophy(NALD)FucosidosisInfantileRefsumDiseaseFatty AcidHydroxylase-AssociatedNeurodegeneration(FAHN)Acute DisseminatedEncephalomyeolitis(ADEM)Cerebral AutosomalDominant Arteriopathywith SubcorticalInfarcts andLeukoencephalopathy(CADASIL)Leukoencephalopathywith Brain Stem andSpinal CordInvolvement andLactate Elevation(LBSL)AlexanderDiseaseGM1GangliosidosisCanavanDiseaseCoats PlusSyndrome orCerebroretinalMicroangiographywith Calcificationsand Cysts(CRMCC)Adult OnsetAutosomalDominantLeukodystrophy(ADLD)Hypomyelinationwith Atrophy ofthe BasalGanglia andCerebellum (H-ABC)OculodentodigitalDysplasia withCerebral WhiteMatterAbnormalities(ODDD)RNAse T2-deficientLeukoencephalopathyRefsumDiseaseGloboid CellLeukodystrophy(KrabbeDisease)PelizaeusMerzbacherDiseaseAcuteHemorrhagicLeukoencephalitis(AHLE)CerebrotendinousXanthomatosis(CTX)Aicardi-GoutieresSyndromeHypomyelinationwithHypogonadotropicHypogonadismand Hypodontia(4H Syndrome)VanishingWhite MatterDisease(VWM)Adrenomyeloneuropathy(AMN)18qSyndromeMetachromaticLeukodystrophy(MLD)GM2Gangliosidosis(Tay-SachsDisease)Hereditary DiffuseLeukoencephalopathywith Spheroids (HDLS)Adrenoleukodystrophy(ALD)ZellwegerSyndromeSjogren-LarssonSyndromeAdultPolyglucosanBodyDiseaseMegalencephalicLeukodystrophywith subcorticalCysts (MLC)FukuyamaCongenitalMuscularDystrophyGalactosialidosisNasu-Hakola Disease(NHD) or PolycysticLipomembranousOsteodysplasia withSclerosingLeukoencephalopathy(PLOSL)NeonatalAdrenoleukodystrophy(NALD)FucosidosisInfantileRefsumDiseaseFatty AcidHydroxylase-AssociatedNeurodegeneration(FAHN)Acute DisseminatedEncephalomyeolitis(ADEM)Cerebral AutosomalDominant Arteriopathywith SubcorticalInfarcts andLeukoencephalopathy(CADASIL)Leukoencephalopathywith Brain Stem andSpinal CordInvolvement andLactate Elevation(LBSL)AlexanderDiseaseGM1GangliosidosisCanavanDiseaseCoats PlusSyndrome orCerebroretinalMicroangiographywith Calcificationsand Cysts(CRMCC)Adult OnsetAutosomalDominantLeukodystrophy(ADLD)Hypomyelinationwith Atrophy ofthe BasalGanglia andCerebellum (H-ABC)OculodentodigitalDysplasia withCerebral WhiteMatterAbnormalities(ODDD)RNAse T2-deficientLeukoencephalopathyRefsumDiseaseGloboid CellLeukodystrophy(KrabbeDisease)PelizaeusMerzbacherDiseaseAcuteHemorrhagicLeukoencephalitis(AHLE)CerebrotendinousXanthomatosis(CTX)Aicardi-GoutieresSyndromeHypomyelinationwithHypogonadotropicHypogonadismand Hypodontia(4H Syndrome)VanishingWhite MatterDisease(VWM)Adrenomyeloneuropathy(AMN)18qSyndromeMetachromaticLeukodystrophy(MLD)GM2Gangliosidosis(Tay-SachsDisease)Hereditary DiffuseLeukoencephalopathywith Spheroids (HDLS)Adrenoleukodystrophy(ALD)ZellwegerSyndromeSjogren-LarssonSyndromeAdultPolyglucosanBodyDiseaseMegalencephalicLeukodystrophywith subcorticalCysts (MLC)FukuyamaCongenitalMuscularDystrophyGalactosialidosis

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