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30 Cards in this Set
- Front
- Back
APC
|
FAP/PKD
|
|
APP
|
Alzheimer Disease
|
|
PSEN1
|
Alzheimer Disease
|
|
PSEN2
|
Alzheimer Disease
|
|
APO e2
|
Alzheimer Disease
|
|
APO e4q
|
Alzheimer Disease
|
|
N-acetylgalactosamine Transferase
|
Blood-type A
|
|
Galactose Transferase
|
Blood-type B
|
|
Type O
|
Single base pair deletion of N-acetylgalactosamine transferase gene
|
|
CBP
|
ATP-dependent chromatin remodeling complex
|
|
CYP3A4
|
Cyp 450 enzyme
|
|
ECE1
|
Hirschprung Disease
|
|
RET
|
Hirschprung Disease
|
|
EDNRB
|
Hirschprung Disease
|
|
SOX10
|
Hirschprung Disease
|
|
MADH
|
Hirschprung Disease
|
|
GDNF
|
Hirschprung Disease
|
|
NRTN
|
Hirschprung Disease
|
|
EDN3
|
Hirschprung Disease
|
|
EP300
|
ATP-Dependent chromatin remodeling complex
|
|
MYST1
|
ATP-Dependent chromatin remodeling complex
|
|
GALT
|
Galactosemia
|
|
HLA-DQ2
|
Diabetes Mellitus
|
|
HLA-DQ6
|
Diabetes Mellitus
|
|
HLA-DQ8
|
Diabetes Mellitus
|
|
16p11.2
|
Copy number variants
Deletion: Obesity Duplication: Underweight |
|
LRP6
|
Cardiovascular Disease
|
|
MEF2A
|
Cardiovascular Disease
|
|
MTHFR
|
Spina Bifida
Cardiovascular Disease |
|
VHL
|
PKD
|