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PHENOTYPE

  • Phenotype
  • Composite of the organism's observable characteristics or traits

    In genetics, the phenotype (from Ancient Greek φαίνω (phaínō) 'to appear, show' and τύπος (túpos) 'mark, type') is the set of observable characteristics

    Phenotype

    Phenotype

    Phenotype

  • Phenotype (disambiguation)
  • Topics referred to by the same term

    Look up phenotype in Wiktionary, the free dictionary. A phenotype is the set of observable characteristics or traits of an organism. Phenotype may also

    Phenotype (disambiguation)

    Phenotype_(disambiguation)

  • Phenotype modification
  • Phenotype modification is the process of experimentally altering an organism's phenotype to investigate the impact of phenotype on the fitness. Phenotype

    Phenotype modification

    Phenotype_modification

  • Thrifty phenotype
  • Theory of prenatal development

    Thrifty phenotype refers to the correlation between low birth weight of neonates and the increased risk of developing metabolic syndromes later in life

    Thrifty phenotype

    Thrifty_phenotype

  • The Extended Phenotype
  • 1982 book by Richard Dawkins

    The Extended Phenotype is a 1982 book by the evolutionary biologist Richard Dawkins, in which the author introduced a biological concept of the same name

    The Extended Phenotype

    The_Extended_Phenotype

  • Genotype–phenotype distinction
  • Distinction made in genetics

    The genotype–phenotype distinction is drawn in genetics. The "genotype" is an organism's full hereditary information. The "phenotype" is an organism's

    Genotype–phenotype distinction

    Genotype–phenotype distinction

    Genotype–phenotype_distinction

  • Phenotype (clinical medicine)
  • Presentation of a disease

    In a nosological sense, the term phenotype can be used in clinical medicine for speaking about the presentation of a disease. The complementary concept

    Phenotype (clinical medicine)

    Phenotype_(clinical_medicine)

  • Hh blood group
  • Rare blood type

    hh, or the Bombay blood group, is a rare blood type. This blood phenotype was first discovered in Bombay by Y. M. Bhende in 1952. It is mostly found in

    Hh blood group

    Hh_blood_group

  • DNA phenotyping
  • DNA profiling technique

    DNA phenotyping is the process of predicting an organism's phenotype using only genetic information collected from genotyping or DNA sequencing. This term

    DNA phenotyping

    DNA phenotyping

    DNA_phenotyping

  • Human Phenotype Ontology
  • The Human Phenotype Ontology (HPO) is a formal ontology of human phenotypes. Developed as part of the Monarch Initiative in collaboration with members

    Human Phenotype Ontology

    Human_Phenotype_Ontology

  • Online Mendelian Inheritance in Man
  • Online catalog of human genes, with a particular focus on the gene-phenotype relationship

    the gene-phenotype relationship. As of 28 June 2019[update], approximately 9,000 of the over 25,000 entries in OMIM represented phenotypes; the rest

    Online Mendelian Inheritance in Man

    Online_Mendelian_Inheritance_in_Man

  • Human physical appearance
  • Look, outward phenotype

    appearance is the outward phenotype or look of human beings. There are functionally infinite variations in human phenotypes, though society reduces the

    Human physical appearance

    Human physical appearance

    Human_physical_appearance

  • Broader autism phenotype
  • Informal classification for people with autistic traits

    The broader autism phenotype (BAP) is an informal classification that covers people who have some traits similar to autism, but who do not meet the diagnostic

    Broader autism phenotype

    Broader_autism_phenotype

  • Allele
  • Variant of DNA sequence at a locus

    will mask the effect of the recessive allele, giving a dominant phenotype. The phenotype of recessive alleles are observable when an organism is homozygous

    Allele

    Allele

  • Wolf–Hirschhorn syndrome
  • Chromosomal deletion syndrome

    distinct craniofacial phenotype and intellectual disability. The most common characteristics include a distinct craniofacial phenotype (microcephaly, micrognathia

    Wolf–Hirschhorn syndrome

    Wolf–Hirschhorn syndrome

    Wolf–Hirschhorn_syndrome

  • Asthma phenotyping and endotyping
  • Medical classification of asthma

    Asthma phenotyping and endotyping is a novel approach to asthma classification inspired by precision medicine. It seeks to separate the clinical presentations

    Asthma phenotyping and endotyping

    Asthma_phenotyping_and_endotyping

  • Adrenoleukodystrophy
  • Genetic neurological disease

    heterogeneous disorder, showing several distinct phenotypes, and no clear pattern of genotype–phenotype correlation. As an X-linked disorder, ALD presents

    Adrenoleukodystrophy

    Adrenoleukodystrophy

    Adrenoleukodystrophy

  • Dominance (genetics)
  • One gene variant masking the effect of another in the other copy of the gene

    (A) phenotype, and the last showing the (a) phenotype, thereby producing the 3:1 phenotype ratio. Mendel did not use the terms gene, allele, phenotype, genotype

    Dominance (genetics)

    Dominance (genetics)

    Dominance_(genetics)

  • Senescence-associated secretory phenotype
  • Phenotype of senescent cells which secrete certain substances

    Senescence-associated secretory phenotype (SASP) is a phenotype associated with senescent cells wherein those cells secrete high levels of inflammatory

    Senescence-associated secretory phenotype

    Senescence-associated_secretory_phenotype

  • Genotype
  • Part of the genetic makeup of a cell which determines one of its characteristics

    contributes to phenotype, the observable traits and characteristics in an individual or organism. The degree to which genotype affects phenotype depends on

    Genotype

    Genotype

    Genotype

  • Mixed-phenotype acute leukemia
  • Mixed-phenotype acute leukemia (MPAL) is a group of blood cancers (leukemia) which have combined features of myeloid and lymphoid cancers. It is a rare

    Mixed-phenotype acute leukemia

    Mixed-phenotype_acute_leukemia

  • Maternal effect
  • Influence of mother's environment and genotype on offspring's phenotype

    A maternal effect is a situation where the phenotype of an organism is determined not only by the environment it experiences and its genotype, but also

    Maternal effect

    Maternal_effect

  • Phenotype (album)
  • 2016 studio album by Textures

    Phenotype is the fifth studio album by Dutch progressive metalcore band Textures. It was released on February 5, 2016, by Nuclear Blast. The album was

    Phenotype (album)

    Phenotype_(album)

  • Digital phenotyping
  • Multidisciplinary field of science

    Digital phenotyping is a multidisciplinary field of science, first defined in a May 2016 paper in JMIR Mental Health authored by John Torous, Mathew V

    Digital phenotyping

    Digital_phenotyping

  • Phenotype microarray
  • Technology for phenotyping of cells

    The phenotype microarray approach is a technology for high-throughput phenotyping of cells. A phenotype microarray system enables one to monitor simultaneously

    Phenotype microarray

    Phenotype_microarray

  • McLeod syndrome
  • Medical condition

    late-onset dementia, and behavioral changes.[citation needed] The McLeod phenotype is a recessive mutation of the Kell blood group system. The McLeod gene

    McLeod syndrome

    McLeod syndrome

    McLeod_syndrome

  • Genotype–phenotype map
  • Conceptual model in genetic architecture

    The genotype–phenotype map is a conceptual model in genetic architecture. Coined in a 1991 paper by Pere Alberch, it models the interdependency of genotype

    Genotype–phenotype map

    Genotype–phenotype map

    Genotype–phenotype_map

  • Mendelian inheritance
  • Type of biological inheritance

    trait in the phenotype (genetic carriers), 25% are homozygous with the recessive trait and therefore express the recessive trait in the phenotype. The genotypic

    Mendelian inheritance

    Mendelian inheritance

    Mendelian_inheritance

  • ABO blood group system
  • Classification of blood types

    and individuals with IBIB or IBi have type B. IAIB people have both phenotypes, because A and B express a special dominance relationship: codominance

    ABO blood group system

    ABO blood group system

    ABO_blood_group_system

  • Arm folding
  • Method of crossing arms

    their arms is a dynamic morphological demonstration of two alternative phenotypes. Once adopted, manner of arms folding across the chest does not change

    Arm folding

    Arm folding

    Arm_folding

  • Directional selection
  • Type of genetic selection favoring one extreme phenotype

    better fitness than individuals with intermediate or opposite extreme phenotypes. Over time, the allele frequencies, and consequently the population mean

    Directional selection

    Directional selection

    Directional_selection

  • Invasion (cancer)
  • Direct extension and penetration by cancer cells into neighboring tissues

    resilient against opposing microenvironmental factors, acquire an aggressive phenotype and the capacity to metastasize. Invasive tumor growth is enabled by the

    Invasion (cancer)

    Invasion (cancer)

    Invasion_(cancer)

  • Mexico
  • Country in North America

    and racism in Mexico have remained in the contemporary era. Although phenotype is not as important as culture, European features and lighter skin tone

    Mexico

    Mexico

    Mexico

  • Phenotype (igneous petrology)
  • In igneous petrology, a phenotype is an aphanitic igneous rock which is identified and classified according to the mineralogy of its phenocrysts, when

    Phenotype (igneous petrology)

    Phenotype_(igneous_petrology)

  • Canalisation (genetics)
  • Measure of the ability of a population to produce the same phenotype

    Canalisation is a measure of the ability of a population to produce the same phenotype regardless of variability of its environment or genotype. It is a form

    Canalisation (genetics)

    Canalisation (genetics)

    Canalisation_(genetics)

  • Rh blood group system
  • Human blood group system involving 49 blood antigens

    gene is usually deleted or otherwise nonfunctional).[citation needed] Rh phenotypes are readily identified through the presence or absence of the Rh surface

    Rh blood group system

    Rh blood group system

    Rh_blood_group_system

  • Replication error phenotype
  • Subgroup of tumors

    The positive replication error phenotype (RER+) defines a subgroup of tumors that have been documented well in Hereditary nonpolyposis colorectal cancer

    Replication error phenotype

    Replication_error_phenotype

  • Phenotypic plasticity
  • Trait change of an organism in response to environmental variation

    learning. The special case when differences in environment induce discrete phenotypes is termed polyphenism. Generally, phenotypic plasticity is more important

    Phenotypic plasticity

    Phenotypic plasticity

    Phenotypic_plasticity

  • Blood type
  • Classification based on antibodies and antigens on RBC surfaces

    serologic tests reporting a direct blood type phenotype, genotyping allows the prediction of a phenotype based on the knowledge of the molecular basis

    Blood type

    Blood type

    Blood_type

  • Molecular phenotyping
  • Molecular phenotyping describes the technique of quantifying pathway reporter genes, i.e. pre-selected genes that are modulated specifically by metabolic

    Molecular phenotyping

    Molecular_phenotyping

  • Mutant
  • Phenotypically-different organism resulting from a mutation

    Wild-type Physcomitrella and knockout mosses: Deviating phenotypes induced in gene-disruption library transformants. Physcomitrella wild-type and transformed

    Mutant

    Mutant

    Mutant

  • Kell antigen system
  • Human blood group classification

    the first described antibodies to K2. The K0 phenotype was first described in 1957 and the McLeod phenotype was found in Hugh McLeod, a Harvard dental student

    Kell antigen system

    Kell_antigen_system

  • Dog
  • Domesticated species of canid

    influenced by those genes which act in the neural crest, which led to the phenotypes observed in modern dogs. There are around 450 official dog breeds, the

    Dog

    Dog

    Dog

  • Botrytis cinerea
  • Species of fungus

    fungicide resistance phenotype known as MDR1. An even higher overexpression yields mrr1 composed partly of Δ497V/L, yielding MDR1h phenotypes with even more

    Botrytis cinerea

    Botrytis cinerea

    Botrytis_cinerea

  • XX male syndrome
  • Congenital condition where an individual with a 46,XX karyotype is male

    condition in which an individual with a 46,XX karyotype develops a male phenotype. In 90 percent of these individuals, the syndrome is caused by the father's

    XX male syndrome

    XX male syndrome

    XX_male_syndrome

  • Expressivity (genetics)
  • Degree to which a phenotype is expressed

    In genetics, expressivity is the degree to which a phenotype is expressed by individuals having a particular genotype. Alternatively, it may refer to

    Expressivity (genetics)

    Expressivity_(genetics)

  • The Selfish Gene
  • 1976 book by Richard Dawkins

    from selection that occurs "at the level of the gene mediated by the phenotype" and that any selection at the group level occurred only under rare circumstances

    The Selfish Gene

    The_Selfish_Gene

  • Lactase persistence
  • Ability to digest milk after infancy

    [clarification needed] The distribution of the lactase persistence (LP) phenotype, or the ability to digest lactose into adulthood, is not homogeneous in

    Lactase persistence

    Lactase_persistence

  • Euthyroid sick syndrome
  • Endocrinological condition

    classical phenotype of this condition is often seen in starvation, critical illness, or patients in the intensive care unit. Similar endocrine phenotypes are

    Euthyroid sick syndrome

    Euthyroid_sick_syndrome

  • Klippel–Feil syndrome
  • Congenital condition characterised by fusion of two or more vertebrae in the neck

    Klippel–Feil syndrome (KFS), also known as cervical vertebral fusion syndrome, is a rare congenital condition characterized by the abnormal fusion of any

    Klippel–Feil syndrome

    Klippel–Feil syndrome

    Klippel–Feil_syndrome

  • Transgressive segregation
  • Process in genetics

    formation of extreme phenotypes, or transgressive phenotypes, observed in segregated hybrid populations compared to phenotypes observed in the parental

    Transgressive segregation

    Transgressive_segregation

  • Pygmy peoples
  • Ethnic group

    height is unusually short. The term pygmyism is used to describe the phenotype of endemic short stature (as opposed to disproportionate dwarfism occurring

    Pygmy peoples

    Pygmy peoples

    Pygmy_peoples

  • Neophyte Phenotype
  • 2001 studio album by Noah23

    Neophyte Phenotype is a 2001 album by Canadian-American alternative hip hop artist Noah23. It features dense wordplay over drum and bass-influenced beats

    Neophyte Phenotype

    Neophyte_Phenotype

  • International Mouse Phenotyping Consortium
  • International Mouse Phenotyping Consortium (IMPC) is an international scientific endeavour to create and characterize the phenotype of 20,000 knockout

    International Mouse Phenotyping Consortium

    International_Mouse_Phenotyping_Consortium

  • Phenocopy
  • Variation in phenotype caused by environmental conditions

    In phenomics, a phenocopy is a variation in phenotype (generally referring to a single trait) which is caused by environmental conditions (often, but

    Phenocopy

    Phenocopy

    Phenocopy

  • Wilhelm Johannsen
  • Danish botanist and geneticist

    physiologist, and geneticist. He is best known for coining the terms gene, phenotype and genotype, and for his 1903 "pure line" experiments in genetics. Johannsen

    Wilhelm Johannsen

    Wilhelm Johannsen

    Wilhelm_Johannsen

  • Transgressive
  • Topics referred to by the same term

    form of verb in some languages Transgressive phenotype, a phenotype that is more extreme than the phenotypes displayed by either of the parents Transgressive

    Transgressive

    Transgressive

  • Natural selection
  • Mechanism of evolution by differential reproduction

    offspring; variation, which partly resulted from an organism's own agency (see phenotype; Baldwin effect); and the struggle for existence, which included both

    Natural selection

    Natural selection

    Natural_selection

  • Baldwin effect
  • Effect of learned behavior on evolution

    is not sufficiently emphasized that the degree of modification of the phenotype is in itself genetically controlled; it is assumed that phenotypic rigidity

    Baldwin effect

    Baldwin effect

    Baldwin_effect

  • Naive T cell
  • T cell which has not yet encountered its cognate antigen

    increasing evidence that naive T cells are actually heterogeneous in phenotype, function, dynamics and differentiation status, resulting in a whole spectrum

    Naive T cell

    Naive_T_cell

  • Dihybrid cross
  • Concept in genetics

    heterozygous individuals will result in predictable ratios for both genotype and phenotype in the offspring. The expected phenotypic ratio of crossing heterozygous

    Dihybrid cross

    Dihybrid cross

    Dihybrid_cross

  • Robustness (evolution)
  • Persistence of a biological trait under uncertain conditions

    called mutation tolerance) describes the extent to which an organism's phenotype remains constant in spite of mutation. Robustness can be empirically measured

    Robustness (evolution)

    Robustness (evolution)

    Robustness_(evolution)

  • Attention deficit hyperactivity disorder
  • Neurodevelopmental disorder

    cyclase. The DRD4–7R mutation results in a wide range of behavioural phenotypes, including ADHD symptoms reflecting split attention. The DRD4 gene is

    Attention deficit hyperactivity disorder

    Attention_deficit_hyperactivity_disorder

  • Fitness (biology)
  • Expected reproductive success

    to a genotype or to a phenotype in a given environment or time. The fitness of a genotype is manifested through its phenotype, which is also affected

    Fitness (biology)

    Fitness_(biology)

  • Human
  • Species of hominid in the genus Homo

    long time inhabited specific climates tend to have developed specific phenotypes that are beneficial for those environments – short stature and stocky

    Human

    Human

    Human

  • Fibroblast growth factor 21
  • Protein-coding gene in mammals

    identified as a genetic mechanism responsible for the sweet tooth behavioral phenotype, a trait associated with cravings for sweets and high sugar consumption

    Fibroblast growth factor 21

    Fibroblast growth factor 21

    Fibroblast_growth_factor_21

  • Phenotype mixing
  • Phenotype mixing is a form of interaction between two viruses each of which holds its own unique genetic material. The two particles "share" coat proteins

    Phenotype mixing

    Phenotype_mixing

  • Citrin deficiency
  • Monogenetic inherited metabolic disease

    disorder. Citrin deficiency is a complex disorder with several age-dependent phenotypes. A hallmark symptom of citrin deficiency is a strong dietary preference

    Citrin deficiency

    Citrin_deficiency

  • Pharmacogenomics
  • Study of the role of the genome in drug response

    limited to monogenic phenotypes (i.e., single gene-drug interactions). Pharmacogenomics refers to polygenic drug response phenotypes and encompasses transcriptomics

    Pharmacogenomics

    Pharmacogenomics

    Pharmacogenomics

  • Pleiotropy
  • Influence of a single gene on multiple phenotypic traits

    effects during development. Selectional pleiotropy occurs when a single phenotype influences evolutionary fitness in multiple ways (depending on factors

    Pleiotropy

    Pleiotropy

    Pleiotropy

  • Albinism
  • Disorder causing lack of pigmentation

    amphibians have focused on mutations in the tyrosinase gene. The albino phenotype of the northern leopard frog (Lithobates pipiens) has been attributed

    Albinism

    Albinism

    Albinism

  • Monohybrid cross
  • Cross between two organisms with different variations at one genetic locus of interest

    will have the dominant allele's phenotype. And the remaining quarter of the F2s will have the recessive allele's phenotype. This predicted 3:1 phenotypic

    Monohybrid cross

    Monohybrid cross

    Monohybrid_cross

  • MASS syndrome
  • Medical condition

    2019.{{cite web}}: CS1 maint: numeric names: authors list (link) "MASS PHENOTYPE". Marfan Foundation. Retrieved 19 February 2018. Jacobs AM, Toudjarska

    MASS syndrome

    MASS syndrome

    MASS_syndrome

  • Neurofibromatosis type II
  • Type of neurofibromatosis disease

    dominant mode of transmission. There are two forms of the NF2: The Wishart-phenotype form is characterized by multiple cerebral and spinal lesions in people

    Neurofibromatosis type II

    Neurofibromatosis type II

    Neurofibromatosis_type_II

  • Phenomics
  • Systematic study of phenotypes

    Phenomics studies phenotypes using phenotyping methods to characterize an organism with a set of traits which changes over time, due to development and

    Phenomics

    Phenomics

  • Caramelo (dog)
  • Mixed-breed dog with socio-environmental typology

    is attributed to alleles that are notably pleiotropic to behavioural phenotypes. Upon domestication, certain traits were targeted by humans for being

    Caramelo (dog)

    Caramelo (dog)

    Caramelo_(dog)

  • Breeding back
  • Artificial selection

    primarily domestic animals, in an attempt to achieve an animal breed with a phenotype that resembles a wild type ancestor, usually one that has gone extinct

    Breeding back

    Breeding back

    Breeding_back

  • Genome-wide association study
  • Study of genetic variants in different individuals

    be people with different phenotypes for a particular trait, for example blood pressure. This approach is known as phenotype-first, in which the participants

    Genome-wide association study

    Genome-wide association study

    Genome-wide_association_study

  • Pneumoridae
  • Family of grasshoppers

    display striking sexual dimorphism, and several species exhibit a dual male phenotype. They are nocturnal, specialized herbivores which (with few exceptions)

    Pneumoridae

    Pneumoridae

    Pneumoridae

  • Monoclonal B-cell lymphocytosis
  • Medical condition

    atypical CLL/SLL, or non-CLL/SLL phenotype based on these cells' expression of certain marker proteins. A fourth MBL phenotype, monoclonal B-cell lymphocytosis-marginal

    Monoclonal B-cell lymphocytosis

    Monoclonal_B-cell_lymphocytosis

  • Chronic obstructive pulmonary disease
  • Lung disease involving long-term poor airflow

    has been suggested that these early phenotypes may reflect unique underlying mechanisms: an "emphysematous phenotype" that involves destruction of air sacs

    Chronic obstructive pulmonary disease

    Chronic obstructive pulmonary disease

    Chronic_obstructive_pulmonary_disease

  • Genetic linkage
  • Aspect of population genetics

    lines.[citation needed] According to Mendelian genetics, the expected phenotypes would occur in a 9:3:3:1 ratio of PL:Pl:pL:pl. To their surprise, they

    Genetic linkage

    Genetic_linkage

  • Quantitative genetics
  • Study of the inheritance of continuously variable traits

    of quantitative traits, which are phenotypes that vary continuously—such as height or mass—as opposed to phenotypes and gene-products that are discretely

    Quantitative genetics

    Quantitative genetics

    Quantitative_genetics

  • Genetic representation
  • Data structure and types for evolutionary computation

    genotype-phenotype mapping: All possible admissible solutions must be contained in the search space. When more possible genotypes exist than phenotypes, the

    Genetic representation

    Genetic representation

    Genetic_representation

  • Leukocyte adhesion deficiency
  • Medical condition

    Leukocyte adhesion deficiency (LAD) is a rare autosomal recessive disorder characterized by immunodeficiency resulting in recurrent infections. LAD is

    Leukocyte adhesion deficiency

    Leukocyte_adhesion_deficiency

  • Glycogen storage disease type V
  • Human disease caused by deficiency of a muscle enzyme

    British physician Brian McArdle of Guy's Hospital, London. In the classic phenotype, the onset of this disease is usually noticed in childhood, but often

    Glycogen storage disease type V

    Glycogen storage disease type V

    Glycogen_storage_disease_type_V

  • Epistasis
  • Dependence of a gene mutation's phenotype on mutations in other genes

    each mutation by itself produces a unique phenotype but the two mutations together show the same phenotype as the gene A mutation, then gene A is epistatic

    Epistasis

    Epistasis

    Epistasis

  • Jews
  • Ethnoreligious group

    2010). "Ashkezani Jews". Molecular Photofitting: Predicting Ancestry and Phenotype Using DNA. Elsevier. p. 383. ISBN 978-0-08-055137-1. Behar, Doron M.;

    Jews

    Jews

    Jews

  • Obligate parasite
  • Type of organism

    to the genes of parasites infecting it. This behaviour is an extended phenotype. Three main evolutionary routes have been suggested for the appearance

    Obligate parasite

    Obligate_parasite

  • Wild type
  • Phenotype of the typical form of a species as it occurs in nature

    The wild type (WT) is the phenotype of the typical form of a species as it occurs in nature. Originally, the wild type was conceptualized as a product

    Wild type

    Wild type

    Wild_type

  • Haploinsufficiency
  • Concept in genetics

    combination with a variant allele is insufficient to produce the wild-type phenotype. Haploinsufficiency may arise from a de novo or inherited loss-of-function

    Haploinsufficiency

    Haploinsufficiency

    Haploinsufficiency

  • Bosch–Boonstra–Schaaf optic atrophy syndrome
  • Medical condition

    shows a clear genotype-phenotype correlation. Patients that have a loss of function variant (e.g. deletions) show a mild phenotype, while patients that

    Bosch–Boonstra–Schaaf optic atrophy syndrome

    Bosch–Boonstra–Schaaf optic atrophy syndrome

    Bosch–Boonstra–Schaaf_optic_atrophy_syndrome

  • Leucism
  • Partial loss of pigmentation in an animal

    "depigmentation") can also result from injury. Leucism is often used to describe the phenotype that results from defects in pigment cell differentiation and/or migration

    Leucism

    Leucism

    Leucism

  • List of OBO Foundry ontologies
  • et al. (November 2016). "The flora phenotype ontology (FLOPO): tool for integrating morphological traits and phenotypes of vascular plants". Journal of Biomedical

    List of OBO Foundry ontologies

    List_of_OBO_Foundry_ontologies

  • Selection limits
  • Animal breeding concept

    directional selection. Genotype-environment interaction occurs when the phenotype produced by a particular set of alleles (at one or more loci) confers

    Selection limits

    Selection limits

    Selection_limits

  • Human leukocyte antigen
  • Genes on human chromosome 6

    clinical situation is often used for identifying HLA phenotypes. An example of an extended phenotype for a person might be: A*01:01/*03:01, C*07:01/*07:02

    Human leukocyte antigen

    Human leukocyte antigen

    Human_leukocyte_antigen

  • White Brazilians
  • Race or color

    citizens who are considered or self-identify as "white" due to their phenotype, often because of European or Levantine ancestry. The main ancestry of

    White Brazilians

    White Brazilians

    White_Brazilians

  • Richard Dawkins
  • British evolutionary biologist and author (born 1941)

    niche construction to be a special case of extended phenotype. The concept of extended phenotype helps explain evolution, but it does not help predict

    Richard Dawkins

    Richard Dawkins

    Richard_Dawkins

  • Punnett square
  • Tabular summary of genetic combinations

    the Punnett square. Phenotypes may be predicted with at least better-than-chance accuracy using a Punnett square, but the phenotype that may appear in

    Punnett square

    Punnett square

    Punnett_square

  • Sex and gender differences in autism
  • Differences in autism diagnosis frequencies with respect to gender

    conceptualisations" of autism. The female autism phenotype differs from the typical male autism phenotype in social relationships, relational interests,

    Sex and gender differences in autism

    Sex_and_gender_differences_in_autism

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Online names & meanings

  • Leif
  • Boy/Male

    Swedish American Norse Scandinavian

    Leif

    Dearly loved.

  • GWENDDYDD
  • Female

    Arthurian

    GWENDDYDD

    , morning-star.

  • Dhairaya
  • Boy/Male

    Gujarati, Indian

    Dhairaya

    Calm; Patience

  • Nangial
  • Boy/Male

    Indian

    Nangial

    Honorable

  • GAVRIIL
  • Male

    Russian

    GAVRIIL

    (Гавриил) Russian form of Greek Gabriēl, GAVRIIL means "man of God" or "warrior of God."

  • Dashan | தஷாந 
  • Boy/Male

    Tamil

    Dashan | தஷாந 

    Ruler, Style....in every thing

  • Charaka
  • Boy/Male

    Hindu, Indian, Sanskrit

    Charaka

    Vagabond; Wanderer

  • Rahas
  • Boy/Male

    Gujarati, Hindu, Indian, Kannada, Malayalam, Marathi, Telugu

    Rahas

    Soft; Secret

  • Beth-haccerem
  • Biblical

    Beth-haccerem

    house of the vineyard

  • Fnam
  • Boy/Male

    Welsh

    Fnam

    Legendary son of Nwyvre.

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