Phenotype

    flowchart
    AA["Associated Authors (2)"]
    C[Phenotype]
    BC["Broader Concepts (1)"]
    NC["Narrower Concepts (66)"]
    C== skos:broader ==>BC
    NC== skos:broader ==>C
    AA== dcterms:relation ==>C
    click BC "#broader-concepts"
    click NC "#narrower-concepts"
    click AA "#associated-authors"

    NI["add incoming edge"]
    NO["add outgoing edge"]
    NI-- ? -->C
    C-- ? -->NO
    click NI "#add-incoming-edge"
    click NO "#add-outgoing-edge"
    style NI stroke-width:2px,stroke-dasharray: 5 5
    style NO stroke-width:2px,stroke-dasharray: 5 5

Wikidata

https://www.wikidata.org/wiki/Q104053

OpenAlex ID

https://openalex.org/C127716648 (API record)

OpenAlex Description

composite of the organism's observable characteristics or traits resulting from the interaction of its genotype with the environment

OpenAlex Level [?]

3

Broader Concepts

• Gene

Narrower Concepts

• ABCA4
• Allelic heterogeneity
• Bardet–Biedl syndrome
• CD11c
• CD163
• CD24
• CD86
• Cellular senescence
• Chromosomal Deletion
• Ciliopathies
• Ciliopathy
• Clinical phenotype
• Complementation
• Compound heterozygosity
• Conditional gene knockout
• Deletion syndrome
• Exome sequencing
• Eye development
• Facial dysmorphism
• Forward genetics
• Frameshift mutation
• Fungal prion
• Gain of function
• Genetic architecture
• Genetic heterogeneity
• Genetic screen
• Genotype-phenotype distinction
• Germline mosaicism
• Global developmental delay
• Haploinsufficiency
• Hereditary spastic paraplegia
• Heritability of autism
• Homeotic gene
• Imaginal disc
• Junctional epidermolysis bullosa (veterinary medicine)
• LMNA
• Limb-girdle muscular dystrophy
• Lineage markers
• Loss function
• M2 Macrophage
• MECP2
• Macrophage polarization
• Mass cytometry
• Melanocortin 1 receptor
• Memory T cell
• Microdeletion syndrome
• Missense mutation
• Nephronophthisis
• Null allele
• OMIM : Online Mendelian Inheritance in Man
• Penetrance
• Peripheral myelin protein 22
• Phase variation
• Phenocopy
• Phenome
• Phenotypic screening
• Phenotypic switching
• Phenotypic trait
• Pleiotropy
• Positional cloning
• Reversion
• Side population
• Suppressor mutation
• Tumor-associated macrophage
• Waardenburg syndrome
• Xq28

Associated Authors

• Anuranjan Anand
• Jenna L Everard

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