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Error in the mendelian inheritance
A Mendelian error in the genetic analysis of a species, describes an allele in an individual which could not have been received from either of its biological
Mendelian_error
Type of biological inheritance
Mendelian inheritance (also known as Mendelism) is a type of biological inheritance following the principles originally proposed by Gregor Mendel in 1865
Mendelian_inheritance
Austrian biologist and friar (1822–1884)
Genetics Mendel Polar Station in Antarctica Mendel University in Brno Mendelian error The Gardener of God, an Italian docudrama about the life and works
Gregor_Mendel
Statistical method in genetic epidemiology
In epidemiology, Mendelian randomization (commonly abbreviated to MR) is a method using measured variation in genes to examine the causal effect of an
Mendelian_randomization
Health problem from genome abnormalities
epidemiology List of genetic disorders Population groups in biomedicine Mendelian error "Genetic Disorders". Learn.Genetics. University of Utah. Archived from
Genetic_disorder
Variant of DNA sequence at a locus
Genealogical DNA test Allele frequency Haploinsufficiency Meiosis Mendelian error Mendelian inheritance Mitosis Penetrance Polymorphism Punnett square Single-nucleotide
Allele
Laboratory process
access the genotype of an individual in various contexts. Mendelian error – Error in the mendelian inheritance Quantitative trait locus – DNA locus associated
Genotyping
Problem with focusing light accurately on the retina due to the shape of the eye
refractive error. Individuals that have parents with certain refractive errors are more likely to have similar refractive errors. The Online Mendelian Inheritance
Refractive_error
One of several alternatives to evolution by natural selection
with work by the mathematician Ronald Fisher. However, the alignment of Mendelian genetics and natural selection began as early as 1902 with a paper by
Mutationism
the museum's exhibition plans. The museum frequently stages short-term art exhibitions. Gregor Mendel Mendel Lectures Mendelian error Official website
Mendel Museum of Masaryk University
Mendel_Museum_of_Masaryk_University
Attempt to explain evolution by forces other than natural selection
fossil record of most of the phyla in the Cambrian explosion was "pre-Mendelian" evolution caused by physical factors. Brian Goodwin, described by Wagner
Structuralism_(biology)
Obsolete theory of genetics
others, soon confirmed that same year by experiments by William Bateson. Mendelian inheritance with segregating, particulate alleles came to be understood
Blending_inheritance
Tabular summary of genetic combinations
traits from the parents. The Punnett square is a visual representation of Mendelian inheritance, a fundamental concept in genetics discovered by Gregor Mendel
Punnett_square
Nepeta cataria; species of plant
caused by a Mendelian-dominant gene. A 2011 pedigree analysis of 210 cats in two breeding colonies (taking into account measurement error by repeated
Catnip
Alteration in the nucleotide sequence of a genome
Mutations result from errors during replication, mitosis, meiosis, or damage to DNA, which then may trigger error-prone repair or cause an error during replication
Mutation
Conceptual model in philosophy of science
trait stability that had led Galton to abandon causality, by resurrecting Mendelian inheritance. In 1921 Wright's path analysis became the theoretical ancestor
Causal_model
Statistical model containing both fixed effects and random effects
A mixed model, mixed-effects model or mixed error-component model is a statistical model containing both fixed effects and random effects. These models
Mixed_model
Fusion of natural selection with Mendelian inheritance
Modern Synthesis. The synthesis combined the ideas of natural selection, Mendelian genetics, and population genetics. It also related the broad-scale macroevolution
Modern synthesis (20th century)
Modern_synthesis_(20th_century)
Concept in genetics
including genetic drift. Ronald Fisher, who explained natural selection using Mendelian genetics, held the view that genetic drift plays at most a minor role
Genetic_drift
Sequencing of all the exons of a genome
whole-genome sequencing. Since these variants can be responsible for both Mendelian and common polygenic diseases, such as Alzheimer's disease, whole exome
Exome_sequencing
Sequence of DNA that determines traits in an organism
In biology, the word gene has two meanings. The Mendelian gene is a basic unit of heredity. The molecular gene is a sequence of nucleotides in DNA that
Gene
Medical condition
Mendelian susceptibility to mycobacterial disease (MSMD) is a rare genetic disease. It is a primary immunodeficiency featured by molecular defects in
Mendelian susceptibility to mycobacterial disease
Mendelian_susceptibility_to_mycobacterial_disease
Statistical measure of how far values spread from their average
his 1918 paper The Correlation Between Relatives on the Supposition of Mendelian Inheritance: The great body of available statistics show us that the deviations
Variance
for change (orthogenesis), and sudden large mutations (saltationism). Mendelian genetics, a series of 19th-century experiments with pea plant variations
History of evolutionary thought
History_of_evolutionary_thought
Medical condition for inability to feel pain
1093/bmb/ldaa003. ISSN 0007-1420. PMC 7227775. PMID 32219415. Online Mendelian Inheritance in Man (OMIM): Insensitivity to Pain, Congenital, with Anhidrosis;
Congenital insensitivity to pain
Congenital_insensitivity_to_pain
Study of collection and analysis of data
seminal paper The Correlation between Relatives on the Supposition of Mendelian Inheritance (which was the first to use the statistical term, variance)
Statistics
Study of health and disease within a population
disease transmissionPages displaying short descriptions of redirect targets Mendelian randomization – Statistical method in genetic epidemiology Occupational
Epidemiology
Study of the human mitochondrial genome
certain circumstances. Mitochondrial inheritance is therefore non-Mendelian, as Mendelian inheritance presumes that half the genetic material of a fertilized
Human_mitochondrial_genetics
Science of genes, heredity and variation
April 2020 at the Wayback Machine on 16 March 2008. Peter J. Bowler, The Mendelian Revolution: The Emergency of Hereditarian Concepts in Modern Science and
Genetics
Inheritance of two copies of one parent's chromosome
on 16 May 2021. Retrieved 29 February 2016. Angelman Syndrome, Online Mendelian Inheritance in Man "OMIM Entry - # 608149 - KAGAMI-OGATA SYNDROME". omim
Uniparental_disomy
that, on its rediscovery in the 1900s, helped to establish the theory of Mendelian inheritance. In ancient Greece, Hippocrates suggested that all organs
History_of_genetics
System for fixing base errors of DNA replication
13310–9. doi:10.1074/jbc.M800606200. PMC 2423938. PMID 18326858. Online Mendelian Inheritance in Man (OMIM): 276300 Bernstein C, Bernstein H (May 2015)
DNA_mismatch_repair
Medical condition
General Medicine (6th ed.). McGraw-Hill. p. 771. ISBN 0-07-138076-0. Online Mendelian Inheritance in Man (OMIM): Ichthyosis hystrix, Curth-Macklin type - 146590
Ichthyosis_hystrix
Protein-coding gene in the species Homo sapiens
Retrieved 2023-08-21. "Mitochondrial pyruvate carrier 1; MPC1". Online Mendelian Inheritance in Man (OMIM). Retrieved 2023-08-21. Pujol C, Lebigot E, Gaignard
Mitochondrial pyruvate carrier 1
Mitochondrial_pyruvate_carrier_1
Medical condition
examples: Online Mendelian Inheritance in Man (OMIM): 311250 - hyperammonemia due to ornithine transcarbamylase deficiency Online Mendelian Inheritance in
Hyperammonemia
Species of flowering plant in the pea and bean family Fabaceae
subject because of its ability to self-pollinate and its easily observed Mendelian traits such as colour, height and petal form. Many genetic principles
Sweet_pea
Absence of the iris, usually involving both eyes
Online Mendelian Inheritance in Man (OMIM): 106210 AN Online Mendelian Inheritance in Man (OMIM): 106220 Aniridia and absent patella Online Mendelian Inheritance
Aniridia
DNA inside the nucleus of eukaryotic cells
mitochondrial DNA and plastid DNA coding for the rest. It adheres to Mendelian inheritance, with information coming from two parents, one male and one
Nuclear_DNA
Application of statistical techniques to biological systems
collected data. In the early 1900s, after the rediscovery of Mendel's Mendelian inheritance work, there were gaps in understanding between genetics and
Biostatistics
Pseudoscientific Soviet biological theory
varying degrees, as did the People's Republic of China for some years. Mendelian genetics, the science of heredity, developed into an experimentally based
Lysenkoism
Partial loss of pigmentation in an animal
dominant white Archived 2009-01-30 at the Wayback Machine at Online Mendelian Inheritance in Animals. An L1 element intronic insertion in the black-eyed
Leucism
Collection of statistical models
population genetics, The Correlation Between Relatives on the Supposition of Mendelian Inheritance. His first application of the analysis of variance to data
Analysis_of_variance
Medical condition
PMC 1648209. PMID 4508182. GLYCOGEN STORAGE DISEASE IXa1; GSD9A1 OMIM — Online Mendelian Inheritance in Man "Definition: glycogen storage disease type VIII from
Glycogen_storage_disease
Obsolete theories in natural history and natural philosophy
supported by experiment, and rendered obsolete by Darwinian evolution and Mendelian genetics, combined in the modern synthesis which finds that genes in the
List of superseded scientific theories
List_of_superseded_scientific_theories
X-linked recessive copper-transport disorder
findings associated with cutaneous conditions Wilson's disease Online Mendelian Inheritance in Man (OMIM): 309400 James, William; Berger, Timothy; Elston
Menkes_disease
Medical condition
(classic galactosemia) is the most common type of galactosemia, an inborn error of galactose metabolism, caused by a deficiency of the enzyme galactose-1-phosphate
Galactose-1-phosphate uridylyltransferase deficiency
Galactose-1-phosphate_uridylyltransferase_deficiency
Digit of a foot
Elsevier/Churchill Livingstone. p. 557. ISBN 978-0-8089-2306-0. Online Mendelian Inheritance in Man (OMIM): Toes – relative lengths of first and second
Toe
Abnormal number or structure of chromosomes
Mb-sized circular DNA molecules found in the nucleus that undergo non-Mendelian inheritance and do not have detectable centromeric activity. A primary
Chromosome_abnormality
Law of Dominance and Uniformity One of three fundamental principles of Mendelian inheritance, which states that different alleles of the same gene may
Glossary of genetics and evolutionary biology
Glossary_of_genetics_and_evolutionary_biology
Longest recorded life span
for his work with the pharmaceutical rapamycin.[better source needed] A mendelian randomization trial in humans found that a 1-standard deviation increase
Maximum_life_span
Scientific study of genes at the molecular level
study is based on the merging of several sub-fields in biology: classical Mendelian inheritance, cellular biology, molecular biology, biochemistry, and biotechnology
Molecular_genetics
Score from a test designed to assess intelligence
(by which he did not mean genes, although he did develop several pre-Mendelian theories of particulate inheritance). He hypothesized that there should
Intelligence_quotient
Principle in genetics
; F | E = 0 , O > 0 {\displaystyle F{\big |}_{E=0,O>0}} is undefined. Mendelian genetics were rediscovered in 1900. However, it remained somewhat controversial
Hardy–Weinberg_principle
Colouration of animal coat/fur
type I (OCA1), TYR-related in Felis catus (domestic cat) - OMIA - Online Mendelian Inheritance in Animals". omia.org. Retrieved 14 February 2026. Cotton
Acromelanism
Mutation in flower species
production of peloric flowers has been shown to generally follow standard Mendelian inheritance, this is not fixed and had been linked to the inability of
Pelorism
Differential transmission of genes residing in the same genome
presence in gametes or offspring above the expected according to fair Mendelian segregation and fair gametogenesis) and altruism (genes in the same genome
Intragenomic_conflict
Genetic point mutation that results in an amino acid change in a protein
Malaria, Resistance to, included. HBB, GLU6VAL — 141900.0243". Online 'Mendelian Inheritance in Man' (OMIM). Yang L, Yu P, Chen X, Cai T (August 2016)
Missense_mutation
Condition in which the head is small due to an underdeveloped brain
Archived from the original on 2020-09-21. Retrieved 2019-07-30. Online Mendelian Inheritance in Man (OMIM): Microcephaly 18, Primary, Autosomal Dominant;
Microcephaly
Period when evolution was widely accepted, but natural selection was not
like Morgan, Bateson, de Vries and others from 1900 to 1915 established Mendelian genetics linked to chromosomal inheritance, which validated August Weismann's
The_eclipse_of_Darwinism
British polymath (1890–1962)
Gregor Mendel and Charles Darwin, as his work used mathematics to combine Mendelian genetics and natural selection; this contributed to the revival of Darwinism
Ronald_Fisher
Meiospore Melanoma Melting of DNA Mendel's first law Mendel's second law Mendelian ratio Merozygote Messenger RNA Met Metabolism Metafemale Metamale Metamere
Index_of_genetics_articles
Scientific hypothesis about inheritance
to disprove Lamarckism, as it did not address use and disuse. Later, Mendelian genetics supplanted the notion of inheritance of acquired traits, eventually
Lamarckism
Medical condition
Hippel–Lindau syndrome at NLM Genetics Home Reference Hippel–Lindau disease at Whonamedit? Online Mendelian Inheritance in Man (OMIM): 608537 (VHL gene)
Von_Hippel–Lindau_disease
Design of tasks
of the 'modern synthesis' that used mathematical models to integrate Mendelian genetics with Darwin's selection theories. To psychologists, Fisher was
Design_of_experiments
Medical condition
GeneReviews. University of Washington, Seattle. Retrieved 2026-04-13. Online Mendelian Inheritance in Man (OMIM): Gluosidase, beta, acid; GBA - 606463 Grabowski
Gaucher's_disease
Group of genetic disorders resulting in fragile bones
as these mutations are inherited in an autosomal dominant pattern of Mendelian inheritance. Those with the rare autosomal recessive forms of OI have
Osteogenesis_imperfecta
Medical condition
PMID 9662398. S2CID 12040233. Online Mendelian Inheritance in Man (OMIM): ACHROMATOPSIA 4; ACHM4 - 613856 Online Mendelian Inheritance in Man (OMIM): CONE
Achromatopsia
Expression of genes depending on parentage
Genomic imprinting is an inheritance process independent of the classical Mendelian inheritance. It is an epigenetic process that involves DNA methylation
Genomic_imprinting
Type of mathematical model
epilepsy, or schizophrenia, cannot be Mendelian diseases because they are common; do not appear in Mendelian ratios; respond slowly to selection against
Threshold_model
Significance of the peppered moth in evolutionary biology
demonstrate that mathematical models that combined natural selection with Mendelian genetics could explain evolution – an effort that played a key role in
Peppered_moth_evolution
Medical condition
Redline, Susan (2022-09-22). Barsh, Gregory S. (ed.). "The impact of Mendelian sleep and circadian genetic variants in a population setting". PLOS Genetics
Familial_natural_short_sleep
Medical condition
100 (25): e150. doi:10.1161/01.cir.100.25.e150. PMID 10604916. Online Mendelian Inheritance in Man (OMIM): Carney Complex, type 1; CNC1 - 160980 "Cardiac
Carney_complex
British family with members with a speech disorder caused by mutations in FOXP2
the first human speech and language disorder known to exhibit strict Mendelian inheritance. Brought to medical attention from their school children in
KE_family
RNA processing within a biological cell
PMC 125535. PMID 11447102. Berg, Tymoczko & Stryer 2007, p. 836 harvnb error: no target: CITEREFBergTymoczkoStryer2008 (help) Shafee, Thomas; Lowe, Rohan
Post-transcriptional modification
Post-transcriptional_modification
Difference in DNA among individuals or populations
paper entitled "The correlation between relatives on the supposition of Mendelian inheritance", R.A. Fisher introduced the statistical concept of variance;
Genetic_variation
Species of plant
Betto-Colliard, C.; Schartl, M.; Moritz, C.; Perrin, N. (2011). "Simultaneous Mendelian and clonal genome transmission in a sexually reproducing, all-triploid
Rosa_canina
Eugenics book by Henry Herbert Goddard
work contains intricately constructed family trees, showing near-perfect Mendelian ratios in the inheritance of negative and positive traits. Goddard recommended
The_Kallikak_Family
Association of several clinically recognizable features
Archived from the original (PDF) on 2011-05-15. McCusick, Victor (1986). Mendelian Inheritance in Man (7th ed.). Baltimore: Johns Hopkins University Press
Syndrome
Doctors who were working for the state, and not for their patients, using a Mendelian type of logic chart, saw extermination of their patients as the correct
List_of_Nazi_doctors
Method of DNA sequencing developed in 1977
DE, Eichler EE (June 2023). "Applications of long-read sequencing to Mendelian genetics". Genome Medicine. 15 (1): 42. doi:10.1186/s13073-023-01194-3
Sanger_sequencing
seminal paper The Correlation between Relatives on the Supposition of Mendelian Inheritance, the first use to use the statistical term, variance. In 1919
History_of_statistics
Aspect of population genetics
self-crossed the resulting PpLl lines.[citation needed] According to Mendelian genetics, the expected phenotypes would occur in a 9:3:3:1 ratio of PL:Pl:pL:pl
Genetic_linkage
Congenital disorder of nervous system
631–670. doi:10.1007/978-0-387-30378-9_26. ISBN 978-0-387-30345-1. Online Mendelian Inheritance in Man (OMIM): Zellweger syndrome; ZS - 214100 Sundaram SS
Zellweger_syndrome
Genetic disorders causing weakness or paralysis from common triggers
diseases include:[citation needed] Hypokalemic periodic paralysis (Online Mendelian Inheritance in Man (OMIM): 170400), where potassium leaks into the muscle
Periodic_paralysis
Lab technique in cellular biology
S, Foley AR, et al. (19 April 2017). "Improving genetic diagnosis in Mendelian disease with transcriptome sequencing". Science Translational Medicine
RNA-Seq
Medical hypothesis
meta-analyses of genetic studies, prospective epidemiologic studies, Mendelian randomization studies, and randomized clinical trials. This evidence base
Lipid_hypothesis
English physician
metabolism and disease. This research, combined with the new understanding of Mendelian inheritance, evolved from an investigation of a few families with an obscure
Archibald_Garrod
Abnormally elevated levels of lipids or lipoproteins in the blood
Pharmacists Association. Archived from the original on 2011-09-27. Online Mendelian Inheritance in Man (OMIM): Apolipoprotein C-II Deficency - 207750 Yamamura
Hyperlipidemia
DNA matching techniques to identify someone's father
television series that debuted in fall 2013 Genetic: Heritability List of Mendelian traits in humans "A Non-invasive Test to Determine Paternity in Pregnancy"
DNA_paternity_testing
Bias in the sampling of a population
deciding if the characteristic is inherited as a simple Mendelian trait. Following the laws of Mendelian inheritance, if the parents in a family do not have
Sampling_bias
Biological system that determines the development of an organism's sex
the inheritance of traits in pea plants. These findings—now known as Mendelian inheritance—introduced the concept of heritable units (genes) passed from
Sex-determination_system
American mathematician (1916–2001)
Harbor Laboratory, in order to develop a mathematical formulation for Mendelian genetics. This research resulted in Shannon's PhD thesis, called An Algebra
Claude_Shannon
Medical condition
carbohydrate-deficient glycoprotein syndrome) is one of several rare inborn errors of metabolism in which glycosylation of a variety of tissue proteins and/or
Congenital disorder of glycosylation
Congenital_disorder_of_glycosylation
Medical condition
doi:10.1016/j.chembiol.2017.04.009. PMC 5482780. PMID 28479296. Online Mendelian Inheritance in Man (OMIM): Methylmalonyl-CoA Epimerase Deficiency - 251120
Methylmalonic_acidemias
Medical condition
Bamshad MJ (January 2010). "Exome sequencing identifies the cause of a mendelian disorder". Nature Genetics. 42 (1): 30–5. doi:10.1038/ng.499. PMC 2847889
Miller_syndrome
Muscular diseases caused by defects in metabolic processes
that primarily affect muscle. They are generally genetic defects (inborn errors of metabolism) that interfere with the ability to create energy, causing
Metabolic_myopathy
Aristotle's theories of biology
Inheritance is thus particulate (definitely one trait or another), as in Mendelian genetics, unlike the Hippocratic model which was continuous and blending
Aristotle's_biology
Medical condition
Hereditary fructose intolerance (HFI) is an inborn error of fructose metabolism caused by a deficiency of the enzyme aldolase B. Individuals affected
Hereditary fructose intolerance
Hereditary_fructose_intolerance
Change in the heritable traits of populations
competing ideas of evolution were refuted and evolution was combined with Mendelian inheritance and population genetics to give rise to modern evolutionary
Evolution
test Mediation (statistics) Medical statistics Medoid Memorylessness Mendelian randomization Meta-analysis Meta-regression Metalog distribution Method
List_of_statistics_articles
MENDELIAN ERROR
MENDELIAN ERROR
Female
Hebrew
(×ֲבִיש×Ö·×’) Hebrew name ABIYSHAG means "my father is a wanderer" or "father of error." In the bible, this is the name of a young girl who cared for David in his old age. Also spelled Avishag.
Boy/Male
German, Polish
Wanderer
Girl/Female
Australian, Teutonic
Wander
Boy/Male
Shakespearean
The Comedy of Errors' Twin brothers, both named Dromio, attendants on the twin Antipholuses....
Boy/Male
Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi
Error-less
Boy/Male
Tamil
Errorless
Boy/Male
Shakespearean
The Comedy of Errors' Father to the twin brothers Antipholus of Ephesus, and Antipholus of Syracuse.
Girl/Female
Hindu, Indian
Without Error
Male
German
Diminutive form of Old High German Wendel, WENDELIN means "a Wend; a wanderer," a term used to refer to migrant Slavs in the sixth century.Â
Boy/Male
Shakespearean
The Comedy of Errors' A merchant of Syracuse.
Boy/Male
Shakespearean
The Comedy of Errors' Duke of Ephesus.
Boy/Male
Shakespearean
The Comedy of Errors' A schoolmaster.
Boy/Male
Hindu
Errorless
Boy/Male
Shakespearean
The Comedy of Errors' Twin brothers, both named Antipholus, sons to Aemelia and Aegion....
Girl/Female
Shakespearean
The Comedy of Errors' Adriana's servant.
Girl/Female
Indian
Goddess Aadisakti: She who Maintains the Rules of Justice without the Slightest Error
Female
Hebrew
(×ֲבִיש×Ö·×’) Variant spelling of Hebrew Abiyshag, AVISHAG means "my father is a wanderer" or "father of error." In the bible, this is the name of a young girl who cared for David in his old age.Â
Surname or Lastname
English
English : of uncertain derivation. The first recorded instance seems to be William Cleike (Yorkshire 1176), but this may well be an error for Clerke. In subsequent records the name is concentrated in Devon; it seems to have been originally a habitational name connected with a piece of land in the parish of Ermington near Plymouth, first recorded in 1278 as Clekeland(e), and still known as Clickland; the names John de Clakelond and Robert Cleaklond occur in this parish in 1332 and 1337 respectively. The place name may be from Old English cleaca ‘stepping stone’, ‘boundary stone’ (of Celtic origin) + land ‘territory’. Compare Clack.Americanized spelling of German Glück (see Gluck).
Girl/Female
Teutonic
Wander.
Boy/Male
Shakespearean
The Comedy of Errors' A merchant.
MENDELIAN ERROR
MENDELIAN ERROR
Boy/Male
Gujarati, Hindu, Indian
The Sun
Male
Hebrew
(× Ö¸×“Ö´×™×¨) Hebrew name NADIR means "oath."
Girl/Female
Tamil
Anurima | அநà¯à®°à¯€à®®à®¾à®‚
Affectionate
Boy/Male
Hindu, Indian, Tamil, Telugu
King; Kind; Roker
Boy/Male
Indian, Sanskrit
Lord of Citra; Wonderful Lord; Moon
Boy/Male
Tamil
Pranith | பà¯à®°à®¾à®£à¯€à®¤Â
Calmness
Boy/Male
Tamil
Anuttam | அநà¯à®¤à¯à®¤à®®Â
Unsurpassed
Boy/Male
Hindu, Indian
Happy
Boy/Male
Hindu
Almighty Lord
Boy/Male
Hindu
The name means quiet person
MENDELIAN ERROR
MENDELIAN ERROR
MENDELIAN ERROR
MENDELIAN ERROR
MENDELIAN ERROR
n.
One who encourages and propagates error; one who holds to error.
n.
A defect; a fault; an error; a blemish; an imperfection; as, the vices of a political constitution; the vices of a horse.
n.
The quality or state of being wrong; wrongfulness; error; fault.
a.
Full of error; wrong.
n.
Any cause of stumbling, perplexity, or error.
n.
A false step; a stumble; a misstep; a loss of footing or balance. Fig.: An error; a failure; a mistake.
a.
Deviation or departure from truth or fact; state of falsity; error; as, to be in the wrong.
n.
The difference between the observed value of a quantity and that which is taken or computed to be the true value; -- sometimes called residual error.
a.
Deceived or misled respecting one's self by one's own mistake or error.
n.
Fig.: That which preserves from corruption or error; that which purifies; a corrective; an antiseptic; also, an allowance or deduction; as, his statements must be taken with a grain of salt.
n.
To adhere to fixed principles; to maintain moral rectitude; to keep from falling into error or vice.
v. t.
To recite (a lesson) or pass (an examination) without an error.
a.
Committing no mistake; incapable or error or failure certain; sure; unfailing; as, the unerring wisdom of God.
a.
Of or pertaining to structure; affecting structure; as, a structural error.
a.
Pertaining to, or discovered by, J. F. Meckel, a German anatomist.
n.
An instrument in writing, under seal, in an epistolary form, issued from the proper authority, commanding the performance or nonperformance of some act by the person to whom it is directed; as, a writ of entry, of error, of execution, of injunction, of mandamus, of return, of summons, and the like.
v. t.
That which fills up, completes, or makes an addition to, something already organized, arranged, or set apart; specifically, a part added to, or issued as a continuation of, a book or paper, to make good its deficiencies or correct its errors.
a.
A true statement; freedom from error of falsehood; adherence to truth or fact.
n.
A wandering or deviation from the right course or standard; irregularity; mistake; inaccuracy; something made wrong or left wrong; as, an error in writing or in printing; a clerical error.
n.
Acknowledgement of a fault; confession of error.