NeonatalAdrenoleukodystrophy(NALD)RefsumDiseasePelizaeusMerzbacherDiseaseLeukoencephalopathywith Brain Stem andSpinal CordInvolvement andLactate Elevation(LBSL)Globoid CellLeukodystrophy(KrabbeDisease)AlexanderDiseaseInfantileRefsumDiseaseHypomyelinationwith Atrophy ofthe BasalGanglia andCerebellum (H-ABC)Sjogren-LarssonSyndromeGM2Gangliosidosis(Tay-SachsDisease)Nasu-Hakola Disease(NHD) or PolycysticLipomembranousOsteodysplasia withSclerosingLeukoencephalopathy(PLOSL)Coats PlusSyndrome orCerebroretinalMicroangiographywith Calcificationsand Cysts(CRMCC)Adrenoleukodystrophy(ALD)MetachromaticLeukodystrophy(MLD)Acute DisseminatedEncephalomyeolitis(ADEM)Fatty AcidHydroxylase-AssociatedNeurodegeneration(FAHN)AdultPolyglucosanBodyDiseaseCanavanDiseaseGalactosialidosisOculodentodigitalDysplasia withCerebral WhiteMatterAbnormalities(ODDD)Adult OnsetAutosomalDominantLeukodystrophy(ADLD)Adrenomyeloneuropathy(AMN)CerebrotendinousXanthomatosis(CTX)GM1GangliosidosisAcuteHemorrhagicLeukoencephalitis(AHLE)Hereditary DiffuseLeukoencephalopathywith Spheroids (HDLS)Cerebral AutosomalDominant Arteriopathywith SubcorticalInfarcts andLeukoencephalopathy(CADASIL)FukuyamaCongenitalMuscularDystrophyFucosidosisZellwegerSyndromeHypomyelinationwithHypogonadotropicHypogonadismand Hypodontia(4H Syndrome)RNAse T2-deficientLeukoencephalopathy18qSyndromeVanishingWhite MatterDisease(VWM)MegalencephalicLeukodystrophywith subcorticalCysts (MLC)Aicardi-GoutieresSyndromeNeonatalAdrenoleukodystrophy(NALD)RefsumDiseasePelizaeusMerzbacherDiseaseLeukoencephalopathywith Brain Stem andSpinal CordInvolvement andLactate Elevation(LBSL)Globoid CellLeukodystrophy(KrabbeDisease)AlexanderDiseaseInfantileRefsumDiseaseHypomyelinationwith Atrophy ofthe BasalGanglia andCerebellum (H-ABC)Sjogren-LarssonSyndromeGM2Gangliosidosis(Tay-SachsDisease)Nasu-Hakola Disease(NHD) or PolycysticLipomembranousOsteodysplasia withSclerosingLeukoencephalopathy(PLOSL)Coats PlusSyndrome orCerebroretinalMicroangiographywith Calcificationsand Cysts(CRMCC)Adrenoleukodystrophy(ALD)MetachromaticLeukodystrophy(MLD)Acute DisseminatedEncephalomyeolitis(ADEM)Fatty AcidHydroxylase-AssociatedNeurodegeneration(FAHN)AdultPolyglucosanBodyDiseaseCanavanDiseaseGalactosialidosisOculodentodigitalDysplasia withCerebral WhiteMatterAbnormalities(ODDD)Adult OnsetAutosomalDominantLeukodystrophy(ADLD)Adrenomyeloneuropathy(AMN)CerebrotendinousXanthomatosis(CTX)GM1GangliosidosisAcuteHemorrhagicLeukoencephalitis(AHLE)Hereditary DiffuseLeukoencephalopathywith Spheroids (HDLS)Cerebral AutosomalDominant Arteriopathywith SubcorticalInfarcts andLeukoencephalopathy(CADASIL)FukuyamaCongenitalMuscularDystrophyFucosidosisZellwegerSyndromeHypomyelinationwithHypogonadotropicHypogonadismand Hypodontia(4H Syndrome)RNAse T2-deficientLeukoencephalopathy18qSyndromeVanishingWhite MatterDisease(VWM)MegalencephalicLeukodystrophywith subcorticalCysts (MLC)Aicardi-GoutieresSyndrome

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