What does CFTD mean?
CFTD means Congenital Fiber-Type Disproportion
This acronym/slang usually belongs to Medical
category.
Particularly in Science Abbreviations, Biomedical Abbreviations, Bioscience Abbreviations, Chromosome Abbreviations, Cytology Abbreviations, Defect Abbreviations, Disease Abbreviations, Disorder Abbreviations, Dna Abbreviations, Molecular biology Abbreviations, Organic chemistry Abbreviations, Pathology Abbreviations
Particularly in Science Abbreviations, Biomedical Abbreviations, Bioscience Abbreviations, Chromosome Abbreviations, Cytology Abbreviations, Defect Abbreviations, Disease Abbreviations, Disorder Abbreviations, Dna Abbreviations, Molecular biology Abbreviations, Organic chemistry Abbreviations, Pathology Abbreviations
What is the abbreviation for Congenital Fiber-Type Disproportion?
Congenital Fiber-Type Disproportion can be abbreviated as CFTD
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Most popular questions people look for before coming to this page
Q: A: |
What does CFTD stand for? CFTD stands for "Congenital Fiber-Type Disproportion". |
Q: A: |
How to abbreviate "Congenital Fiber-Type Disproportion"? "Congenital Fiber-Type Disproportion" can be abbreviated as CFTD. |
Q: A: |
What is the meaning of CFTD abbreviation? The meaning of CFTD abbreviation is "Congenital Fiber-Type Disproportion". |
Q: A: |
What is CFTD abbreviation? One of the definitions of CFTD is "Congenital Fiber-Type Disproportion". |
Q: A: |
What does CFTD mean? CFTD as abbreviation means "Congenital Fiber-Type Disproportion". |
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What is shorthand of Congenital Fiber-Type Disproportion? The most common shorthand of "Congenital Fiber-Type Disproportion" is CFTD. |
Abbreviations or Slang with similar meaning
- CDA I - Congenital Dyserythropoietic Anaemia Type I
- CDAN2 - Congenital Dyserythropoietic Anemia, Type II
- CDAN3 - Congenital Dyserythropoietic Anemia, Type III
- CDG-Ia - Congenital Disorder of Glycosylation Type Ia
- CMS2A - Congenital Myasthenic Syndrome, Type IIA
- CFTDM - Congenital Fiber-Type Disproportion Myopathy
- CNS-FT - Congenital Nephrotic Syndrome of Finnish Type
- CSNB1 - Congenital Stationary Night Blindness, Type 1
- CSNB2 - Congenital Stationary Night Blindness Type 2
- RCM I - Recessive Congenital Methemoglobinemia Type I
- T1FP - Type 1 Fiber Predominance
- CDA1 - Congenital Dyserythropoietic Anemia, type I
- CCA - Cataract, Congenital, Cerulean type
- CCA1 - Cataract, Congenital, Cerulean Type, 1
- CCV - Cataract, Congenital, Volkmann Type
- CFTD - Congenital Fiber-Type Disproportion Myopathy
- TFC - Type Fiber Converter
- CFTD - congenital fibre type disproportion
- CNF - congenital nephrosis of the Finnish type
- CNF - congenital nephrotic syndrome of Finnish type