cpt2 | Carnitine palmitoyltransferase II deficiency

Keyword	CPC	PCC	Volume	Score	Length of keyword
cpt2	1.05	0.6	9384	47	4

Keyword	CPC	PCC	Volume	Score
cpt2	0.67	0.9	9436	35
cpt2 deficiency	1.67	0.9	5457	1
cpt2 diet	1.98	0.6	6058	85
cpt20	0.16	0.3	2729	28
cpt2 placement test unc	1.22	0.8	2756	60
cpt2 disease	0.84	0.7	937	95
cpt2023	1.86	0.1	9491	94
cpt2024	1.92	0.8	1697	48
cpt2 gene	1.52	0.3	3802	12
cpt205	0.56	0.9	6291	9
cpt ii codes	0.96	0.3	4657	85
cpt 20610	0.51	1	1351	39
cpt20 form	1.58	0.7	9815	91
cpt203	1.37	0.7	3460	61
cpt2 antibody	1.59	0.5	8947	77
cpt2 deficiency treatment	0.32	0.1	475	93
cpt2022	1.27	0.6	6731	12
cpt 27447	1.63	0.6	9099	16
cpt2 disease treatment	0.02	0.3	5212	4
cpt2 gene reviews	0.1	0.8	3165	29
cpt2 deficiency diet	1.86	0.2	3001	12

Search Results related to cpt2 on Search Engine

Carnitine palmitoyltransferase II deficiency - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Carnitine_palmitoyltransferase_II_deficiency

WebEndocrinology. Carnitine palmitoyltransferase II deficiency, sometimes shortened to CPT-II or CPT2, is an autosomal recessively inherited genetic metabolic disorder characterized by an enzymatic defect that prevents long-chain fatty acids from being transported into the mitochondria for utilization as an energy source.

DA: 4 PA: 71 MOZ Rank: 99

Carnitine palmitoyltransferase II deficiency - About the Disease
nih.gov

https://rarediseases.info.nih.gov/diseases/1121/carnitine-palmitoyltransferase-ii-deficiency/

WebDisease at a Glance. Summary. Carnitine palmitoyltransferase 2 (CPT2) deficiency is a condition that prevents the body from using certain fats for energy, particularly during periods without food (fasting). There are three main types of CPT2 deficiency: a lethal neonatal form, a severe infantile hepatocardiomuscular form, and a myopathic form.

DA: 47 PA: 100 MOZ Rank: 100

Carnitine Palmitoyltransferase Deficiency | Cedars-Sinai
cedars-sinai.org

https://www.cedars-sinai.org/health-library/diseases-and-conditions/c/carnitine-palmitoyl-transferase-deficiency.html

WebKey points about carnitine palmitoyltransferase deficiency. CPT deficiency is a condition that causes muscle weakness and other symptoms. It happens because of a problem with one of two enzymes, CPT1 or CPT2. The condition is caused by an abnormal gene. Symptoms can include muscle pain and weakness.

DA: 21 PA: 76 MOZ Rank: 84

Carnitine palmitoyltransferase II - Wikipedia
wikipedia.org

https://en.wikipedia.org/wiki/Carnitine_palmitoyltransferase_II

WebCarnitine palmitoyltransferase II precursor (CPT2) is a mitochondrial membrane protein which is transported to the mitochondrial inner membrane. CPT2 together with carnitine palmitoyltransferase I oxidizes long-chain fatty acids in the mitochondria.

DA: 14 PA: 16 MOZ Rank: 43

Carnitine Palmitoyltransferase II Deficiency - GeneReviews®
nih.gov

https://www.ncbi.nlm.nih.gov/books/NBK1253/

WebAug 27, 2004 · USA.gov. Carnitine palmitoyltransferase II (CPT II) deficiency is a disorder of long-chain fatty-acid oxidation. The three clinical presentations are lethal neonatal form, severe infantile hepatocardiomuscular form, and myopathic form (which is usually mild and can manifest from infancy to adulthood).

DA: 80 PA: 12 MOZ Rank: 29

Carnitine palmitoyltransferase II deficiency - MedlinePlus
medlineplus.gov

https://medlineplus.gov/genetics/condition/carnitine-palmitoyltransferase-ii-deficiency/

WebDescription. Carnitine palmitoyltransferase II (CPT II) deficiency is a condition that prevents the body from using certain fats for energy, particularly during periods without food (fasting). There are three main types of CPT II deficiency: a lethal neonatal form, a severe infantile hepatocardiomuscular form, and a myopathic form.

DA: 92 PA: 2 MOZ Rank: 41

Muscle Carnitine Palmitoyltransferase II (CPT II) Deficiency: A
nih.gov

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221885/

WebApr 13, 2020 · Carnitine palmitoyltransferase (CPT) catalyzes the transfer of long- and medium-chain fatty acids from cytoplasm into mitochondria, where oxidation of fatty acids takes place. Deficiency of CPT enzyme is associated with …

DA: 29 PA: 41 MOZ Rank: 13

CPT2 gene: MedlinePlus Genetics
medlineplus.gov

https://medlineplus.gov/genetics/gene/cpt2/

WebThe most common CPT2 gene mutation replaces the protein building block (amino acid) serine with the amino acid leucine at position 113 (written as Ser113Leu or S113L) in the enzyme. This mutation accounts for about 60 percent of the mutations that cause the myopathic form of CPT II deficiency.

DA: 77 PA: 29 MOZ Rank: 73

Carnitine palmitoyltransferase 2 deficiency - National …
rarediseases.org

https://rarediseases.org/gard-rare-disease/carnitine-palmitoyltransferase-2-deficiency/

WebDisease Overview. Carnitine palmitoyltransferase 2 (CPT2) deficiency is a condition that prevents the body from using certain fats for energy, particularly during periods without food (fasting).

DA: 83 PA: 79 MOZ Rank: 35

Carnitine palmitoyltransferase II deficiency with a focus on …
nature.com

https://www.nature.com/articles/s10038-018-0530-z

WebDec 4, 2018 · 16 Citations. Metrics. Abstract. Carnitine palmitoyltransferase (CPT) II deficiency is one of the most common forms of mitochondrial fatty acid oxidation disorder. Its clinical phenotypes...

DA: 96 PA: 24 MOZ Rank: 8