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Mammalian protein found in Homo sapiens
from congenital deficiency, low factor X levels may occur occasionally in a number of disease states. For example, factor X deficiency may be seen in amyloidosis
Factor_X
Medical condition
Factor X deficiency (X as Roman numeral ten) is a bleeding disorder characterized by a lack in the production of factor X (FX), an enzyme protein that
Factor_X_deficiency
Medical condition
Factor XII deficiency is a deficiency in the production of factor XII (FXII), a plasma glycoprotein and clotting factor that participates in the coagulation
Factor_XII_deficiency
Process of formation of blood clots
coagulation factor disorders are the hemophilias. The three main forms are hemophilia A (factor VIII deficiency), hemophilia B (factor IX deficiency or "Christmas
Coagulation
Glycoprotein produced in the stomach which binds to vitamin B12
autoantibodies directed against intrinsic factor or parietal cells themselves lead to an intrinsic factor deficiency, malabsorption of vitamin B12, and subsequent
Intrinsic_factor
Genetic X-linked recessive bleeding disorder
mutation of the gene for factor IX, and resulting in a deficiency of factor IX. It is less common than factor VIII deficiency (haemophilia A). Haemophilia
Haemophilia_B
Abnormally high platelet count in the blood
Other causes of reactive thrombocythemia include: post surgery, iron deficiency, drugs, and rebound effect after bone marrow suppression. Research suggests
Thrombocythemia
Factor II deficiency Factor V deficiency Factor V Leiden mutation Factor VII deficiency Factor VIII deficiency Factor X deficiency, congenital Factor
List_of_diseases_(F)
Abnormality of blood coagulation increasing the risk of blood clotting (thrombosis)
medical science, antithrombin deficiency, was identified in 1965, while the most common abnormalities (including factor V Leiden) were described in the
Thrombophilia
Mammalian protein found in humans
contrast to most other coagulation factors, it is not enzymatically active but functions as a cofactor. Factor V deficiency leads to predisposition for hemorrhage
Factor_V
Lack of red blood cells due to vitamin B12 deficiency
refers to a type of vitamin B12 deficiency anemia that results from lack of intrinsic factor. Lack of intrinsic factor is most commonly due to an autoimmune
Pernicious_anemia
Condition involving impaired blood clotting ability
clotting factors or coagulation factors. Genetic disorders, such as hemophilia and Von Willebrand disease, can cause a reduction in clotting factors. Anticoagulants
Coagulopathy
Serine protease
homologous to the corresponding bond cleaved during factor XI activation. Hereditary deficiencies in PK are very rare. They can cause a prolonged APTT
Prekallikrein
Medical condition
antecedent (PTA) deficiency or Rosenthal syndrome) is a mild form of haemophilia affecting both sexes, due to factor XI deficiency. It predominantly
Haemophilia_C
Disorder resulting from low blood levels of vitamin B12
Vitamin B12 deficiency, also known as cobalamin deficiency, is the medical condition in which the blood and tissues have a lower than normal level of vitamin
Vitamin_B12_deficiency
Complex that catalyzes conversion of prothrombin to thrombin
Congenital factor X deficiency is also extremely rare, affecting an estimated 1 in 1,000,000. A point mutation in the gene encoding factor V can lead
Prothrombinase
Protein involved in coagulation
Factor IX (EC 3.4.21.22) is one of the serine proteases involved in coagulation; it belongs to peptidase family S1. Deficiency of this protein causes haemophilia
Factor_IX
Mammalian protein found in humans
IX and X.[citation needed] The gene for factor VII is located on chromosome 13 (13q34). Factor VII deficiency (congenital proconvertin deficiency) is rare
Factor_VII
Medical condition
Glucose-6-phosphate dehydrogenase deficiency (G6PDD), also known as favism, is the most common enzyme deficiency anemia worldwide. It is an inborn error
Glucose-6-phosphate dehydrogenase deficiency
Glucose-6-phosphate_dehydrogenase_deficiency
Medical condition
Properdin deficiency is a rare X-linked disease in which properdin, an important complement factor responsible for the stabilization of the alternative
Properdin_deficiency
Medical condition
growth hormone receptor deficiency (GHRD), is an autosomal recessive disorder characterized by a lack of insulin-like growth factor 1 (IGF-1; somatomedin-C)
Laron_syndrome
Human disorder
Vitamin D deficiency or hypovitaminosis D is a vitamin D level that is below normal. It most commonly occurs in people when they have inadequate exposure
Vitamin_D_deficiency
High tendency to bleed due to a blood clotting disorder
coagulopathy include anticoagulation with warfarin, liver failure, vitamin K deficiency and disseminated intravascular coagulation. Additionally, the hemotoxic
Bleeding_diathesis
Medical condition
results from a lack of factor I or factor H, two proteins that are key for the regulation of C3. Both primary and secondary C3 deficiency are characterized
Complement_3_deficiency
Mammalian protein involved in blood clotting
trials. Factor XII deficiency is a rare disorder that is inherited in an autosomal recessive manner. Unlike other clotting factor deficiencies, factor XII
Factor_XII
Class of enzymes
factor XIII may be used to identify and classify malignant diseases involving these cells. Factor XIII Deficiency is also known as Laki–Lorand factor
Factor_XIII
Human disease
Thiamine deficiency is a medical condition of low levels of thiamine (vitamin B1). A severe and chronic form is known as beriberi. The name beriberi was
Thiamine_deficiency
Medical condition
hemophilia A) is a blood clotting disorder caused by a genetic deficiency in clotting factor VIII, thereby resulting in significant susceptibility to bleeding
Haemophilia_A
American doctor
H.; High, K. A.; Lively, M. O. (1993-03-15). "Human coagulation factor X deficiency caused by a mutant signal peptide that blocks cleavage by signal
Katherine_A._High
Protein found in humans
in children with severe IGF1 deficiency. Cyclic glycine-proline (cGP) is a metabolite of hormone insulin-like growth factor-1 (IGF1). It has a cyclic structure
Insulin-like_growth_factor_1
Medical condition
resemble GH deficiency, including the childhood growth failure, facial appearance, delayed bone age, and low insulin-like growth factor-1 (IGF-1) levels
Growth_hormone_deficiency
Medical condition
rises first, since the activated Factor VII is the first to "disappear." In later stages of deficiency, the other factors (which have longer half-lives)
Vitamin_K_deficiency
Condition of low level of magnesium in the body
Magnesium deficiency is an electrolyte disturbance in which there is a low level of magnesium in the body. Symptoms include tremor, poor coordination,
Magnesium_deficiency
Blood-clotting protein
Copper is a required cofactor for factor VIII and copper deficiency is known to increase the activity of factor VIII. Factor VIII is on the World Health Organization's
Factor_VIII
kininogen deficiency with diminished levels of plasminogen proactivator and prekallikrein associated with abnormalities of the Hageman factor-dependent
High-molecular-weight kininogen
High-molecular-weight_kininogen
Mammalian protein found in Homo sapiens
this exposes the factor IX binding site of the third apple domain, allowing factor XI's protease activity on it. Deficiency of factor XI causes the rare
Factor_XI
Spectrum of blood disorders
in circulating liver enzymes, bleeding due to factor X deficiency), gastrointestinal track deficiencies (malabsorption), and amyloid deposition in surface
Plasma_cell_dyscrasias
Medical condition
Hypoprothrombinemia is a rare blood disorder in which a deficiency in immunoreactive prothrombin (Factor II), produced in the liver, results in an impaired
Hypoprothrombinemia
Medical condition
Fibrinogen deficiency, also known as factor I deficiency, is a rare inherited bleeding disorder related to fibrinogen function in the coagulation cascade
Fibrinogen_deficiency
Reduced ability of blood to carry oxygen
donation. Causes of decreased production include iron deficiency, folate deficiency, vitamin B12 deficiency, thalassemia and a number of bone marrow tumors
Anemia
Mode of inheritance
blood clotting disorder caused by a mutation of the Factor VIII gene and leading to a deficiency of Factor VIII. It was once thought to be the "royal disease"
X-linked recessive inheritance
X-linked_recessive_inheritance
Rare type of immunodeficiency disease
Nuclear factor-kappa B Essential Modulator (NEMO) deficiency syndrome is a rare type of primary immunodeficiency disease that has a highly variable set
NEMO_deficiency_syndrome
CARD11 deficiency MST1 deficiency TCRα deficiency LCK deficiency IL-21 deficiency IL-21R deficiency UNC119 deficiency NIK deficiency OX40 deficiency IKBKB
List of primary immunodeficiencies
List_of_primary_immunodeficiencies
Disease resulting from a lack of vitamin C
scorbutus is a deficiency disease (state of malnutrition) resulting from a lack of vitamin C (ascorbic acid). Early symptoms of deficiency include weakness
Scurvy
Medical condition
P14 deficiency is a rare autosomal recessive disease characterized as a primary immunodeficiency syndrome. This disease was first identified within a white
P14_deficiency
Metabolic disorder
phenolic neurotransmitter. The deficiency may cause symptoms like flushing, tachycardia, and depression, and be a risk factor for disorders like autism, migraine
Phenol sulfur transferase deficiency
Phenol_sulfur_transferase_deficiency
Medical condition caused by receiving too little or too many nutrients
too many nutrients, resulting in health problems. Specifically, it is a deficiency, excess, or imbalance of energy, protein and other nutrients which adversely
Malnutrition
Impaired physical and mental development due to insufficient iodine intake
Congenital hypothyroidism due to iodine deficiency (ICD-11), or congenital iodine deficiency syndrome (CIDS, ICD-10), is a medical condition present at
Congenital hypothyroidism due to iodine deficiency
Congenital_hypothyroidism_due_to_iodine_deficiency
Insufficient level of copper in the body, leading to anaemia and nervous symptoms
Copper deficiency, or hypocupremia, is defined as insufficient copper to meet the body's needs, or as a serum copper level below the normal range. Symptoms
Copper_deficiency
Insufficient body levels of zinc
Zinc deficiency is defined either as insufficient body levels of zinc to meet the needs of the body, or as a zinc blood level below the normal range. However
Zinc_deficiency
Medical condition
venous thrombosis. Some risk factors for deep vein thrombosis or pulmonary embolism in patients with protein S deficiency include pregnancy, older age
Protein_S_deficiency
Medical condition
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (CAH) is a genetic disorder characterized by impaired production of cortisol in the adrenal
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Congenital_adrenal_hyperplasia_due_to_21-hydroxylase_deficiency
Medical condition
Vitamin deficiency is the condition of a long-term lack of a vitamin. When caused by not enough vitamin intake it is classified as a primary deficiency, whereas
Vitamin_deficiency
Lack of or compromised immune system
functions can be related to illnesses such as X-Linked Agammaglobulinemia and Common Variable Immune Deficiency Secondary immunodeficiencies, also known as
Immunodeficiency
Health condition
of UV exposure. Pregnancy also poses as another high risk factor for vitamin D deficiency. The status levels of vitamin D during the last stages of pregnancy
Vitamin D deficiency in Australia
Vitamin_D_deficiency_in_Australia
Type of blood plasma screening test
distinguish factor deficiencies from factor inhibitors, such as lupus anticoagulant, or specific factor inhibitors, such as antibodies directed against factor VIII
Mixing_study
Medical condition
5α-Reductase 2 deficiency (5αR2D) is an autosomal recessive condition caused by mutations impairing the function of SRD5A2, a gene located on chromosome
5α-Reductase_2_deficiency
Genetic disease involving blood clotting
a recessive X-linked genetic disorder resulting in a deficiency of functional clotting Factor VIII. Haemophilia B is also a recessive X-linked genetic
Haemophilia
Abnormally low level of folate (vitamin B9) in the body
Increased homocysteine levels may suggest deficiency state, but it is also affected by other factors. Vitamin B12 deficiency must be ruled out, if left untreated
Folate_deficiency
Medical condition
Deficiency of Adenosine deaminase 2 (DADA2) is a monogenic disease associated with systemic inflammation and vasculopathy that affects a wide variety of
Adenosine deaminase 2 deficiency
Adenosine_deaminase_2_deficiency
Medical condition
from factors other than mutations in the AR coding region, an unidentified coactivator protein, enzyme deficiencies such as 21-hydroxylase deficiency, or
Androgen insensitivity syndrome
Androgen_insensitivity_syndrome
Australian season of television series
The X Factor is an Australian television reality music competition, based on the original UK series, to find new singing talent; the winner of which received
The X Factor (Australian TV series) season 3
The_X_Factor_(Australian_TV_series)_season_3
Mammalian protein found in Homo sapiens
namely the activated forms of Factor X (Xa), Factor IX (IXa), Factor XI (XIa), Factor XII (XIIa) and, to a greater extent, Factor II (thrombin) (IIa), and
Antithrombin
Reduced ability of the blood to carry oxygen due to a lack of iron
Iron-deficiency anemia is anemia caused by a lack of iron. Anemia is defined as a decrease in the number of red blood cells or the amount of hemoglobin
Iron-deficiency_anemia
Class of enzymes
infections as in patients with Factor D deficiency. PDB: 1HFD Narayana SV, Carson M, el-Kabbani O, Kilpatrick JM, Moore D, Chen X, Bugg CE, Volanakis JE, DeLucas
Factor_D
Medication
and children with hemophilia A or B with inhibitors, congenital factor VII deficiency, and Glanzmann's thrombasthenia with refractoriness to platelet
Recombinant_factor_VIIa
Medical condition
Bevers EM, Comfurius P, Hemker HC, von Dieijen G, Weiss HJ, et al. Impaired factor X and prothrombin activation associated with decreased phospholipid exposure
Scott_syndrome
X-linked dominant genetic disorder
ribonucleoprotein 1) gene on the X chromosome. This results in silencing (methylation) of this part of the gene and a deficiency of the resultant protein (FMRP)
Fragile_X_syndrome
Medical condition
nutritional deficiency. Similarly, folk wisdom also maintained that pica reflected an appetite to compensate for nutritional deficiencies, such as low
Pagophagia
Chemical compound and essential nutrient
and confusion. In Western countries, chronic alcoholism is a risk factor for deficiency. Also at risk are older adults, persons with HIV/AIDS or diabetes
Thiamine
Derivative of folic acid used in cancer treatment
colorectal cancer and pancreatic cancer, and may be used to treat folate deficiency, anemia, and methanol poisoning. It is taken by mouth, injection into
Folinic_acid
Mammalian protein involved in blood clotting
bleeding diathesis. In the 1950s, vWD was shown to be caused by a plasma factor deficiency (instead of being caused by platelet disorders), and, in the 1970s
Von_Willebrand_factor
Medical condition
accept that the cause of KBD is multifactorial, selenium deficiency being the underlying factor that predisposes the target cells (chondrocytes) to oxidative
Kashin–Beck_disease
Medical condition
needed] While inherited deficiencies in uroporphyrinogen decarboxylase often lead to the development of PCT, several risk factors can both cause and exacerbate
Porphyria_cutanea_tarda
Medical condition
Cortisone reductase deficiency is caused by dysregulation of the 11β-hydroxysteroid dehydrogenase type 1 enzyme (11β-HSD1), otherwise known as cortisone
Cortisone reductase deficiency
Cortisone_reductase_deficiency
Enzyme involved in blood coagulation in humans
congenital form of Factor II deficiency, which should not be confused with the prothrombin G20210A mutation, which is also called the factor II mutation. Prothrombin
Thrombin
Vitamin used in animal cell metabolism
disease, inherited intrinsic factor deficiency, and radiation enteritis affecting the distal ileum. Age is also a contributing factor: elderly individuals are
Vitamin_B12
Medical condition
X-linked ichthyosis (abbreviated XLI) is a skin condition caused by the hereditary deficiency of the steroid sulfatase (STS) enzyme that affects 1 in
X-linked_ichthyosis
Group of vitamins
needed] In cases of severe deficiency, B vitamins, especially B12, may also be delivered by injection to reverse deficiencies.[unreliable medical source
B_vitamins
Disease caused by lack of dietary vitamin E
Vitamin E deficiency is a rare condition caused by low levels of vitamin E that may result from malabsorption disorders (such as abetalipoproteinemia,
Vitamin_E_deficiency
Medical condition
which is caused by FoxP3 transcription factor dysfunction. In addition to IPEX-like symptoms, CD25 deficiency increases susceptibility to viral infections
CD25_deficiency
Disorder resulting in severe swelling
inhibits plasma kallikrein, factor XIIa, and factor XIIf. However, in hereditary angioedema with C1 inhibitor deficiency, C1 inhibitor is either reduced
Hereditary_angioedema
Small size of an organism, caused by growth deficiency or genetic mutations
a genetic disorder whereby the limbs are diminutive. Growth hormone deficiency is responsible for most other cases. There are many other less common
Dwarfism
Medical condition
of adrenocorticotropic hormone deficiency. The TBX19 gene, formerly known as TPIT, encodes a T-box transcription factor found in pituitary cells that express
Adrenocorticotropic hormone deficiency
Adrenocorticotropic_hormone_deficiency
Medical condition
JAK3 (Janus kinase 3) deficiency is a dysfunction in cytokine receptor signalling and their production of cytokines. JAK3 is a tyrosine protein kinase
Janus_kinase_3_deficiency
Decreased ability to see color or color differences
Color blindness or color vision deficiency (CVD) is the decreased ability to see color, differences in color, or distinguish shades of color. The severity
Color_blindness
Medical condition
thiamine (vitamin B1). The condition is part of a larger group of thiamine deficiency disorders that includes beriberi, in all its forms, and alcoholic Korsakoff
Wernicke_encephalopathy
Protein found in humans
x. PMID 10620119. Retrieved 28 August 2017. Ruseva MM, Takahashi M, Fujita T, Pickering MC (April 2014). "C3 dysregulation due to factor H deficiency
Complement_component_3
Chemical compound and essential nutrient
biotin deficiency, meaning deficiency due to too little biotin in the diet, is rare because biotin is contained in many foods. Subclinical deficiency can
Biotin
C13of46 Gene and Protein
are restricted to the testis. LINC00454 has been associated with Factor X Deficiency while LINC00452 has been found to promote ovarian carcinogenesis
C13orf46
Medical condition
tumor. Growth hormone deficiency is almost certain if all other pituitary tests are also abnormal, and insulin-like growth factor 1 (IGF-1) levels are
Hypopituitarism
Metabolic disorders in which porphyrins build up in the body
the specific mutation. Hepatic porphyrias are those in which the enzyme deficiency occurs in the liver. Hepatic porphyrias include acute intermittent porphyria
Porphyria
Metalloprotease enzyme
doi:10.1046/j.1538-7836.2003.00169.x. PMID 12871390. S2CID 26485194. Remuzzi G (April 2003). "Is ADAMTS-13 deficiency specific for thrombotic thrombocytopenic
ADAMTS13
Medical condition
protein S deficiency, activated protein C resistance (Factor V Leiden) and antithrombin III deficiency. Although the above hypothesis is the most commonly
Warfarin_necrosis
Thrombophilia Due to Protein C Deficiency, Autosomal Dominant; THPH3". omim.org. Retrieved 2018-03-01. "OMIM Entry - # 300263 - SIDERIUS X-LINKED MENTAL RETARDATION
List_of_genetic_disorders
Lack of androgen hormones in the body
and is dependent on various factors including androgen receptor abundance, sensitivity and function. Androgen deficiency is associated with lack of energy
Androgen_deficiency
Vitamin, dietary supplement, and yellow food dye
identified to be the factor necessary for preventing pellagra, but that was later confirmed to be due to niacin (vitamin B3) deficiency. The confusion was
Riboflavin
Medical condition
Manco-Johnson MJ (November 2008). "Protein C deficiency". Haemophilia. 14 (6): 1214–1221. doi:10.1111/j.1365-2516.2008.01838.x. PMID 19141162. S2CID 2979452. Woźniak
Purpura_fulminans
Medication
as factor IX complex, sold under the brand name Kcentra among others, is a combination medication made up of blood clotting factors II, IX, and X(3-factor
Prothrombin complex concentrate
Prothrombin_complex_concentrate
Medical condition
Vitamin K deficiency bleeding (VKDB) of the newborn, previously known as haemorrhagic disease of the newborn, is a rare form of bleeding disorder that
Vitamin_K_deficiency_bleeding
FACTOR X-DEFICIENCY
FACTOR X-DEFICIENCY
Surname or Lastname
English
English : habitational name from places called Caistor, in Lincolnshire and Norfolk, Caister in Norfolk, or Castor in Cambridgeshire, all named with Old English cæster ‘Roman fort or town’.
Male
Greek
(ΚάστωÏ) Greek name KASTOR means "beaver." In mythology, Castor/Kastor and Pollux/Polydeukes ("very sweet") are the twin sons of Leda and are known as the Gemini twins.
Male
Arthurian
, sir Hector de Maris; (defender).
Male
Spanish
Spanish form of Roman Latin Victor, VÃCTOR means "conqueror."
Surname or Lastname
French and Italian
French and Italian : occupational name from French, northern Italian sartor ‘tailor’ (Latin sartor).English : topographic name denoting someone who lived on land which had been cleared for cultivation, Old French assart, essart ‘woodland cleared for cultivation’ + the habitational suffix -er.
Boy/Male
English American
Doctor; teacher.
Male
English
 Anglicized form of Scottish Gaelic Eachann, HECTOR means "brown horse." Compare with another form of Hector.
Male
Spanish
Spanish form of Latin Hector, H�CTOR means "defend; hold fast."
Boy/Male
Latin
Son of Azeus.
Male
French
 French and German name derived from Occitan astor, ASTOR means "goshawk," itself from Latin acceptor, a variant of accipiter, meaning "hawk." It was originally a derogatory term for men with hawk-like, predatory characteristics.
Male
Greek
(ÎαχώÏ) Greek form of Hebrew Nachowr, NACHOR means "snoring" or "snorting." In the bible, this is the name of the son of Terah and brother of Abraham.
Surname or Lastname
English (chiefly Northamptonshire)
English (chiefly Northamptonshire) : probably from the obsolete slang term facer, denoting a braggart or bully. The earliest citation for this term in OED is c. 1515.Americanized spelling of German Feeser.
Surname or Lastname
English, Portuguese, Galician, Spanish, Catalan, and French
English, Portuguese, Galician, Spanish, Catalan, and French : occupational name for a shepherd, Anglo-Norman French pastre (oblique case pastour), Portuguese, Galician, Spanish, Catalan, pastor ‘shepherd’, from Latin pastor, an agent derivative of pascere ‘to graze’. The religious sense of a spiritual leader was rare in the Middle Ages, and insofar as it occurs at all it seems always to be a conscious metaphor; it is unlikely, therefore, that this sense lies behind any examples of the surname.German and Dutch : humanistic name, a Latinized form of various vernacular names meaning ‘shepherd’, for example Hirt or Schäfer (see Schafer).Americanized spelling of Hungarian Pásztor, an occupational name from pásztor ‘shepherd’.
Male
Icelandic
Perhaps a modern form of Icelandic Fylkir, FALKOR means "people, tribe."Â
Male
English
English surname transferred to forename use, ACTON means "oak tree settlement."Â
Surname or Lastname
Scottish
Scottish : Anglicized form of the Gaelic personal name Eachann (earlier Eachdonn, already confused with Norse Haakon), composed of the elements each ‘horse’ + donn ‘brown’.English : found in Yorkshire and Scotland, where it may derive directly from the medieval personal name. According to medieval legend, Britain derived its name from being founded by Brutus, a Trojan exile, and Hector was occasionally chosen as a personal name, as it was the name of the Trojan king’s eldest son. The classical Greek name, HektÅr, is probably an agent derivative of Greek ekhein ‘to hold back’, ‘hold in check’, hence ‘protector of the city’.German, French, and Dutch : from the personal name (see 2 above). In medieval Germany, this was a fairly popular personal name among the nobility, derived from classical literature. It is a comparatively rare surname in France.
Male
Spanish
Spanish name derived from Latin Pastor, PASTOR means "shepherd." St. Pastor was a 9-year-old boy who along with his 13-year-old brother, Justus, was martyred at Alcalá de Henares in the early 4th century.
Surname or Lastname
Southern French and German
Southern French and German : from Occitan astor ‘goshawk’ (from Latin acceptor, variant of accipiter ‘hawk’), used as a nickname characterizing a predacious or otherwise hawklike man. The name was taken to southwestern Germany by 17th-century Waldensian refugees from their Alpine valleys above Italian Piedmont.English : variant spelling of Aster.Astor is the name of a famous American family of industrialists and newspaper owners. John Jacob Astor I (1763–1848) was born at Walldorf near Heidelberg, Germany, the son of a butcher. He followed his brother Henry to New York and made a fortune in the fur trade, which was greatly increased by his descendants in industry, hotels, and newspapers. They built the Waldorf-Astoria Hotel in New York. The great-grandson of John Jacob I, William Waldorf Astor (1848–1919), moved to England in 1890, becoming an influential newspaper proprietor and taking British citizenship in 1899. In 1917 he was created Viscount Astor of Hever. His son, the 2nd Viscount (1879–1952), married Nancy Shaw (née Langhorne) (1879–1964), daughter of a VA planter. She became the first woman to sit in the British House of Commons as a member of Parliament.
Surname or Lastname
English
English : habitational name from any of several places, especially in Shropshire and adjacent counties, named Acton. Generally, these are from Old English Äc ‘oak’ + tÅ«n ‘settlement’.
Male
English
Roman Latin name VICTOR means "conqueror."Â
FACTOR X-DEFICIENCY
FACTOR X-DEFICIENCY
Girl/Female
Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Sanskrit, Tamil, Telugu
Goddess Parvati
Girl/Female
Hindu
In music. in beat
Girl/Female
Indian, Sikh
Soft; Beautiful
Girl/Female
Muslim
Beautiful, Bright, Brilliant, Shining
Boy/Male
British, English
From the King's Meadow
Girl/Female
Indian
Male
Egyptian
, father of Pesahi, a priest of Amen.
Girl/Female
Tamil
Anukampa | அநà¯à®•à®®à¯à®ªà®¾
Gods grace
Girl/Female
German, Teutonic
Warrior
Girl/Female
Indian
Mind, Intellect, Leader
FACTOR X-DEFICIENCY
FACTOR X-DEFICIENCY
FACTOR X-DEFICIENCY
FACTOR X-DEFICIENCY
FACTOR X-DEFICIENCY
v. i.
Hesitation; trembling; feebleness; an uncertain or broken sound; as, a slight falter in her voice.
n.
A symbol representing ten units, as 10, x, or X.
n.
A name given to the factors of a continued product when the former are derivable from one and the same function F(x) by successively imparting a constant increment or decrement h to the independent variable. Thus the product F(x).F(x + h).F(x + 2h) . . . F[x + (n-1)h] is called a factorial term, and its several factors take the name of factorials.
n.
A contrivance for removing superfluous ink or coloring matter from a roller. See Doctor, 4.
n.
Same as Radius vector.
n.
The body of factors in any place; as, a chaplain to a British factory.
v. t.
To resolve (a quantity) into its factors.
n.
One who transacts business for another; an agent; a substitute; especially, a mercantile agent who buys and sells goods and transacts business for others in commission; a commission merchant or consignee. He may be a home factor or a foreign factor. He may buy and sell in his own name, and he is intrusted with the possession and control of the goods; and in these respects he differs from a broker.
v. t.
To confer a doctorate upon; to make a doctor.
n.
A species of armadillo of the genus Xenurus (X. unicinctus and X. hispidus); the tatouay.
v. t.
To tamper with and arrange for one's own purposes; to falsify; to adulterate; as, to doctor election returns; to doctor whisky.
n.
A building, or collection of buildings, appropriated to the manufacture of goods; the place where workmen are employed in fabricating goods, wares, or utensils; a manufactory; as, a cotton factory.
n.
Same as Fetor.
n.
A doer or actor; particularly, an evil doer; a scoundrel.
imp. & p. p.
of Factor
adv.
In fact; by the act or fact.
n.
A house or place where factors, or commercial agents, reside, to transact business for their employers.
pl.
of Factum
n.
See Faitour.