Tay-Sachs Disease BINGO Cards - Print Free or Customize

Print free Tay-Sachs Disease BINGO cards or modify, no signin required, unlimited cards! Choose from 13,100+ designs or use the bingo card generator. Add numbers, words, pictures, or any combination. Play using PDF prints, digital bingo cards, and the digital bingo caller, or go hybrid.

Tay-Sachs Disease

1 in 200 carriers	AAV vectors	Adult TSD = low HexA levels	Adult TSD = very aggressive	Aspiration pneumonia
Autosomal-dominant	Autosomal-recessive	Benign lipid accumulation	Bernard Tay	Blood-brain barrier
c.533 G > A	c.533 G > R	c.553 G > A	Catalytic dysfunction	Cherry-red spot
Chromosome 15q13.3	Chromosome 15q23	Chromosome 5q23	Enzyme reduction therapy	Flexible loop
Founder effect	Glucose metabolic disorder	GLUT1	Glycosphingolipid	GM2 association protein

Basic Print Title Cell Card Color Image Misc 🔍

Find Setting
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Card Title Title is shown on top of each bingo card. It can be text or an image. If the image is >50kb, then it will be compressed and may loose transparency.
Audio Separator If words on a line are separated by this text, then: The text on the right side of the separator will be spoken by the online game play. Bingo card will only show the text on the left side of the separator. The pdf call list will show the full text. To disable this feature, clear this field.	Audio Mode ON
Quiz Separator If words on a line are separated by this text, then: Bingo card will only show the text on the right side of the separator. The pdf call list will show the full text. To disable this feature, clear this field.	Quiz Mode ON
Grid Items AI Helper Enter numbers, words or phrases, each one on a new line. Column Mode: To specify word lists per column, separate each word list by -c- in a line by itself. Example 1 in 200 carriers AAV vectors Adult TSD = low HexA levels Adult TSD = very aggressive Aspiration pneumonia Autosomal-dominant Autosomal-recessive Benign lipid accumulation Bernard Tay Blood-brain barrier c.533 G > A c.533 G > R c.553 G > A Catalytic dysfunction Cherry-red spot Chromosome 15q13.3 Chromosome 15q23 Chromosome 5q23 Enzyme reduction therapy Flexible loop Founder effect Glucose metabolic disorder GLUT1 Glycosphingolipid GM2 association protein GM2 ganglioside accumulation GM2 ganglioside depletion GM2-gangliosidosis GM3 ganglioside accumulation GM3-gangliosidosis Gross deletion HEXA = chromosome 5 HexA = lysosomal lipase enzyme HexA synthesizes GM2 gangliosides HexA α-subunit mutation HexA β-subunit mutation HEXB = chromosome 15 HexB deficiency Homodimeric HPβCD Hydrolysis Hypermyelination Infantile onset = 4 months old Infantile TSD = high HexA levels iPSC cells Isozymes Juvenile TSD = most severe Lysosomal storage metabolic disorder Mechanical ventilation Microglia Miglustat Missense mutations N-acetylglucosamine N-acetylneuraminic acid Neuronal cells Partial deletions PP6D5 polymer Protein metabolic disorder Proteolytic processing Rigid loop Sex-linked Silencing mutation Toxic lipid accumulation Warren Sachs α-hexosaminidase A αR424 β-hexosaminidase A β-hexosaminidase B Sort \| No Dups
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Similar Bingo Cards: Biology, Genetics, Medical

About: Dive into the intricate world of Tay-Sachs disease and related metabolic disorders with this bingo card designed for genetics students, medical professionals, or rare disease awareness events. The terms featured capture key genetic concepts, disease mechanisms, and diagnostic markers, making it perfect for anyone looking to learn or teach about lysosomal storage diseases in an engaging way.

How To: To save a printable PDF, click the Print button. You can modify the card quantity and other printing settings on the Print tab. Grid items and free space text can be added on the Basic tab. Appearance can be totally personalized on the corresponding tabs, or you can easily find any setting using the 🔍 tab.

How to play Tay-Sachs Disease BINGO Cards?

Virtual Caller: Click on the Play button above.
Printed Players: Print PDF bingo cards and physically scratch the cards.
Virtual Players: Click on the Play button above, and then click on the 🎫 button.
Printed Caller: Print PDF calling list & calling slips and physically draw the slips.
Combo Play: Select any combination above. For example, caller can be either Printed or Virtual. And players can be Printed or Virtual or a mix of both.

Step-By-Step:

Start by saving the Tay-Sachs Disease BINGO PDF by clicking on the "Print" button above.
Open the PDF and print it.
For random calling, you can print another copy of the call list, cut, fold and then pull them randomly at play time.
Cut the bingo cards at the cut lines if there are more than 1 bingo cards per page.
Give one card to each player. For marking, you can use pens. Crayons cost the least.
Select one person to be the caller. If you are playing in a small group, the caller may as well play along with their own Bingo card.
The caller initiates the play by randomly picking an item from the call list and announcing it to all players.
The players look at their cards to see if they have the called word. If they do, they dab that word.
The first player to finish a horizontal, vertical, or a diagonal line of marked items announces "Bingo!" and wins the play.
The caller confirms that the items marked form a correct line according to the Bingo card and call list.
You can play for varied patterns or a full card blackout for a longer play.

This Tay-Sachs Disease BINGO Cards Game contains following Words or Phrases: 1 in 200 carriers, AAV vectors, Adult TSD = low HexA levels, Adult TSD = very aggressive, Aspiration pneumonia, Autosomal-dominant, Autosomal-recessive, Benign lipid accumulation, Bernard Tay, Blood-brain barrier, c.533 G > A, c.533 G > R, c.553 G > A, Catalytic dysfunction, Cherry-red spot, Chromosome 15q13.3, Chromosome 15q23, Chromosome 5q23, Enzyme reduction therapy, Flexible loop, Founder effect, Glucose metabolic disorder, GLUT1, Glycosphingolipid, GM2 association protein, GM2 ganglioside accumulation, GM2 ganglioside depletion, GM2-gangliosidosis, GM3 ganglioside accumulation, GM3-gangliosidosis, Gross deletion, HEXA = chromosome 5, HexA = lysosomal lipase enzyme, HexA synthesizes GM2 gangliosides, HexA α-subunit mutation, HexA β-subunit mutation, HEXB = chromosome 15, HexB deficiency, Homodimeric, HPβCD, Hydrolysis, Hypermyelination, Infantile onset = 4 months old, Infantile TSD = high HexA levels, iPSC cells, Isozymes, Juvenile TSD = most severe, Lysosomal storage metabolic disorder, Mechanical ventilation, Microglia, Miglustat, Missense mutations, N-acetylglucosamine, N-acetylneuraminic acid, Neuronal cells, Partial deletions, PP6D5 polymer, Protein metabolic disorder, Proteolytic processing, Rigid loop, Sex-linked, Silencing mutation, Toxic lipid accumulation, Warren Sachs, α-hexosaminidase A, αR424, β-hexosaminidase A, β-hexosaminidase B.

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