heterozygous


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het·er·o·zy·gous

 (hĕt′ər-ə-zī′gəs)
adj.
1. Having different alleles at one or more corresponding chromosomal loci.
2. Of or relating to a heterozygote.

het′er·o·zy·gos′i·ty (-ə-rō-zī-gŏs′ĭ-tē) n.
American Heritage® Dictionary of the English Language, Fifth Edition. Copyright © 2016 by Houghton Mifflin Harcourt Publishing Company. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.

heterozygous

(ˌhɛtərəʊˈzaɪɡəs)
adj
(Genetics) (of an organism) having different alleles for any one gene: heterozygous for eye colour. Compare homozygous
Collins English Dictionary – Complete and Unabridged, 12th Edition 2014 © HarperCollins Publishers 1991, 1994, 1998, 2000, 2003, 2006, 2007, 2009, 2011, 2014

het•er•o•zy•gous

(ˌhɛt ər əˈzaɪ gəs)

also het•er•o•zy•got•ic

(-ə roʊ zaɪˈgɒt ɪk)

adj.
1. having dissimilar pairs of genes for any hereditary characteristic.
2. of or pertaining to a heterozygote.
(hetero- + Greek -zygos having a yoke]
het`er•o•zy•gos′i•ty (-ə roʊ zaɪˈgɒs ɪ ti) n.
Random House Kernerman Webster's College Dictionary, © 2010 K Dictionaries Ltd. Copyright 2005, 1997, 1991 by Random House, Inc. All rights reserved.

het·er·o·zy·gous

(hĕt′ər-ə-zī′gəs)
Having a contrasting pair of genes, as for tallness and shortness, at corresponding positions on the chromosomes of an organism. Compare homozygous.
The American Heritage® Student Science Dictionary, Second Edition. Copyright © 2014 by Houghton Mifflin Harcourt Publishing Company. Published by Houghton Mifflin Harcourt Publishing Company. All rights reserved.

heterozygous

Possessing two different alleles of a particular gene.
Dictionary of Unfamiliar Words by Diagram Group Copyright © 2008 by Diagram Visual Information Limited
ThesaurusAntonymsRelated WordsSynonymsLegend:
Adj.1.heterozygous - having dissimilar alleles at corresponding chromosomal loci; "heterozygous for eye color"
genetic science, genetics - the branch of biology that studies heredity and variation in organisms
homozygous - having identical alleles at corresponding chromosomal loci; "these two fruit flies are homozygous for red eye color"
Based on WordNet 3.0, Farlex clipart collection. © 2003-2012 Princeton University, Farlex Inc.
Translations
heterozygot
heterozygoot
References in periodicals archive ?
Seven black SA patients, strongly suspected clinically to have FA and heterozygous for the c.637-643delTACCGCC mutation, were investigated.
Distributions of Mediterranean fever mutations Distribution of Mediterranean fever mutations % E148Q heterozygous 7.3 A744S heterozygous 2.8 V726A heterozygous 1.7 R761H heterozygous 0.7 M694I heterozygous 0.7 M694V heterozygous 0.3 M680I/C heterozygous 0.3 R653H heterozygous 0.3 R408Q heterozygous 0.3 M694I heterozygous 0.3 69S heterozygous 0.3 F479L V726A compound heterozygous 0.3 E167D + F479L compound heterozygous 0.3 Table 4.
Red cells with uniform elliptical shape come under the category of hereditary elliptocytosis (HE) however homozygous or compound heterozygous for HE present with distorted morphology termed as hereditary pyeropoikilocytosis (HPP)2.
These are mostly compound heterozygous missense mutations that affect the receptor binding or signal transduction (Chevrier et al., 2011).
Other issues come up in diagnosis of HbS traits where low quantity of HbS is associated with negative sickling test and while diagnosing certain compound heterozygous states such as, for HbD and HbE, HbS and [beta]-thalassaemia, HbS and HbD.
M2 EQUITYBITES-January 9, 2017-Esperion begins three pivotal Phase 3 studies of bempedoic acid in heterozygous familial, hypercholesterolemia and statin intolerant patients
M2 PHARMA-January 9, 2017-Esperion begins three pivotal Phase 3 studies of bempedoic acid in heterozygous familial, hypercholesterolemia and statin intolerant patients
DNA sequence analysis of FOXC1 shows a homozygous mutation c.1139_1141dupGCG(p.Gly380_Ala381insGly) (Figure 5) and a heterozygous mutation c.1359_1361dupCGG(p.Gly456_Gln457insGly) (Figure 6) in all subjects.
Autosomal dominant PCD is caused by heterozygous (monoallelic) mutations in PROC and has an incidence of 1 in 200-500.
A heterozygous polymorphism in exon 3 of NPHS1, c.349G>A (p.Glu117Lys), was identified in patient 1.
Prothrombotic workups including protein C activity, protein S activity, antithrombin III level, APC resistance, lupus anticoagulant, anticardiolipin antibodies, factor VIII inhibitor screening, and factor V Leiden defect were all negative, except for heterozygous mutation for prothrombin G20210A; the d-dimer level was normal 0.14 mcg/mL (0-0.5) and coagulation tests revealed low FVIII levels.
At current prices, PCSK9 inhibitors are not cost effective for patients with heterozygous familial hypercholesterolemia or atherosclerotic cardiovascular disease, according to an analysis published Aug.