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Androgen insensitivity syndrome and Mild androgen insensitivity syndrome

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between Androgen insensitivity syndrome and Mild androgen insensitivity syndrome

Androgen insensitivity syndrome vs. Mild androgen insensitivity syndrome

Androgen insensitivity syndrome (AIS) is an intersex condition in which there is a partial or complete inability of many cells in the affected genetic male to respond to androgenic hormones. Mild androgen insensitivity syndrome (MAIS) is a condition that results in a mild impairment of the cell's ability to respond to androgens.

Similarities between Androgen insensitivity syndrome and Mild androgen insensitivity syndrome

Androgen insensitivity syndrome and Mild androgen insensitivity syndrome have 49 things in common (in Unionpedia): Androgen, Androgen receptor, Body shape, Complete androgen insensitivity syndrome, Dihydrotestosterone, Epididymis, Genetic code, Genetic testing, Glutamine, Glycine, Hepatocellular carcinoma, Hypospadias, Infertility, Intellectual disability, Karyotype, Luteinizing hormone, Male infertility, Mesonephric duct, Meta-analysis, Micropenis, Microsatellite, Mutation, Neurodegeneration, Nucleotide, Paramesonephric duct, Partial androgen insensitivity syndrome, Phenotype, Polyglutamine tract, Prostate, Prostate cancer, ..., Protein folding, Puberty, Quigley scale, Sample size determination, Scrotum, Secondary sex characteristic, Seminal vesicle, Sex organ, Sexual differentiation, Spermatogenesis, Spinal and bulbar muscular atrophy, Symptomatic treatment, Terminal hair, Testosterone, Transcription (biology), Trinucleotide repeat disorder, Urethra, Vas deferens, 5α-Reductase deficiency. Expand index (19 more) »

Androgen

An androgen (from Greek andr-, the stem of the word meaning "man") is any natural or synthetic steroid hormone which regulates the development and maintenance of male characteristics in vertebrates by binding to androgen receptors.

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Androgen receptor

The androgen receptor (AR), also known as NR3C4 (nuclear receptor subfamily 3, group C, member 4), is a type of nuclear receptor that is activated by binding any of the androgenic hormones, including testosterone and dihydrotestosterone in the cytoplasm and then translocating into the nucleus.

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Body shape

Human body shape is a complex phenomenon with sophisticated detail and function.

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Complete androgen insensitivity syndrome

Complete androgen insensitivity syndrome (CAIS) is a condition that results in the complete inability of the cell to respond to androgens.

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Dihydrotestosterone

Dihydrotestosterone (DHT), or 5α-dihydrotestosterone (5α-DHT), also known as androstanolone or stanolone, is an endogenous androgen sex steroid and hormone.

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Epididymis

The epididymis (plural: epididymides or) is a tube that connects a testicle to a vas deferens in the male reproductive system.

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Genetic code

The genetic code is the set of rules used by living cells to translate information encoded within genetic material (DNA or mRNA sequences) into proteins.

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Genetic testing

Genetic testing, also known as DNA testing, allows the determination of bloodlines and the genetic diagnosis of vulnerabilities to inherited diseases.

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Glutamine

Glutamine (symbol Gln or Q) is an α-amino acid that is used in the biosynthesis of proteins.

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Glycine

Glycine (symbol Gly or G) is the amino acid that has a single hydrogen atom as its side chain.

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Hepatocellular carcinoma

Hepatocellular carcinoma (HCC) is the most common type of primary liver cancer in adults, and is the most common cause of death in people with cirrhosis.

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Hypospadias

Hypospadias is a congenital disorder of the urethra where the urinary opening is not at the usual location on the head of the penis.

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Infertility

Infertility is the inability of a person, animal or plant to reproduce by natural means.

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Intellectual disability

Intellectual disability (ID), also known as general learning disability, and mental retardation (MR), is a generalized neurodevelopmental disorder characterized by significantly impaired intellectual and adaptive functioning.

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Karyotype

A karyotype is the number and appearance of chromosomes in the nucleus of a eukaryotic cell.

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Luteinizing hormone

Luteinizing hormone (LH, also known as lutropin and sometimes lutrophin) is a hormone produced by gonadotropic cells in the anterior pituitary gland.

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Male infertility

Male infertility refers to a male's inability to cause pregnancy in a fertile female.

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Mesonephric duct

The mesonephric duct (also known as the Wolffian duct, archinephric duct, Leydig's duct or nephric duct) is a paired organ found in mammals including humans during embryogenesis.

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Meta-analysis

A meta-analysis is a statistical analysis that combines the results of multiple scientific studies.

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Micropenis

Micropenis is an unusually small penis.

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Microsatellite

A microsatellite is a tract of repetitive DNA in which certain DNA motifs (ranging in length from 1–6 or more base pairs) are repeated, typically 5–50 times.

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Mutation

In biology, a mutation is the permanent alteration of the nucleotide sequence of the genome of an organism, virus, or extrachromosomal DNA or other genetic elements.

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Neurodegeneration

Neurodegeneration is the progressive loss of structure or function of neurons, including death of neurons.

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Nucleotide

Nucleotides are organic molecules that serve as the monomer units for forming the nucleic acid polymers deoxyribonucleic acid (DNA) and ribonucleic acid (RNA), both of which are essential biomolecules within all life-forms on Earth.

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Paramesonephric duct

Paramesonephric ducts (or Müllerian ducts) are paired ducts of the embryo that run down the lateral sides of the urogenital ridge and terminate at the sinus tubercle in the primitive urogenital sinus.

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Partial androgen insensitivity syndrome

Partial androgen insensitivity syndrome (PAIS) is a condition that results in the partial inability of the cell to respond to androgens.

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Phenotype

A phenotype is the composite of an organism's observable characteristics or traits, such as its morphology, development, biochemical or physiological properties, behavior, and products of behavior (such as a bird's nest).

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Polyglutamine tract

A polyglutamine tract or polyQ tract is a portion of a protein consisting of a sequence of several glutamine units.

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Prostate

The prostate (from Ancient Greek προστάτης, prostates, literally "one who stands before", "protector", "guardian") is a compound tubuloalveolar exocrine gland of the male reproductive system in most mammals.

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Prostate cancer

Prostate cancer is the development of cancer in the prostate, a gland in the male reproductive system.

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Protein folding

Protein folding is the physical process by which a protein chain acquires its native 3-dimensional structure, a conformation that is usually biologically functional, in an expeditious and reproducible manner.

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Puberty

Puberty is the process of physical changes through which a child's body matures into an adult body capable of sexual reproduction.

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Quigley scale

The Quigley scale is a descriptive, visual system of phenotypic grading that uses seven classes between "fully masculinized" and "fully feminized" genitalia.

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Sample size determination

Sample size determination is the act of choosing the number of observations or replicates to include in a statistical sample.

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Scrotum

The scrotum is an anatomical male reproductive structure that consists of a suspended dual-chambered sack of skin and smooth muscle that is present in most terrestrial male mammals and located under the penis.

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Secondary sex characteristic

Secondary sex characteristics are features that appear during puberty in humans, and at sexual maturity in other animals.

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Seminal vesicle

The seminal vesicles (glandulae vesiculosae), vesicular glands, or seminal glands, are a pair of simple tubular glands posteroinferior to the urinary bladder of some male mammals.

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Sex organ

A sex organ (or reproductive organ) is any part of an animal's body that is involved in sexual reproduction.

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Sexual differentiation

Sexual differentiation is the process of development of the differences between males and females from an undifferentiated zygote.

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Spermatogenesis

Spermatogenesis is the process by which haploid spermatozoa develop from germ cells in the seminiferous tubules of the testis.

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Spinal and bulbar muscular atrophy

Spinal and bulbar muscular atrophy (SBMA), popularly known as Kennedy's disease, is a progressive debilitating neurodegenerative disorder resulting in muscle cramps and progressive weakness due to degeneration of motor neurons in the brainstem and spinal cord.

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Symptomatic treatment

Symptomatic treatment is any medical therapy of a disease that only affects its symptoms, not its cause, i.e., its etiology.

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Terminal hair

Terminal hairs are thick, long, and dark, as compared with vellus hair.

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Testosterone

Testosterone is the primary male sex hormone and an anabolic steroid.

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Transcription (biology)

Transcription is the first step of gene expression, in which a particular segment of DNA is copied into RNA (especially mRNA) by the enzyme RNA polymerase.

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Trinucleotide repeat disorder

Trinucleotide repeat disorders (also known as trinucleotide repeat expansion disorders, triplet repeat expansion disorders or codon reiteration disorders) are a set of genetic disorders caused by trinucleotide repeat expansion, a kind of mutation where trinucleotide repeats in certain genes or intronsDavid W. Sanders & Clifford P. Brangwynne (2017), Nature, 546, 215–216 (08 June 2017) exceed the normal, stable threshold, which differs per gene.

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Urethra

In anatomy, the urethra (from Greek οὐρήθρα – ourḗthrā) is a tube that connects the urinary bladder to the urinary meatus for the removal of urine from the body.

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Vas deferens

The vas deferens (Latin: "carrying-away vessel"; plural: vasa deferentia), also called ductus deferens (Latin: "carrying-away duct"; plural: ductus deferentes), is part of the male reproductive system of many vertebrates; these vasa transport sperm from the epididymis to the ejaculatory ducts in anticipation of ejaculation.

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5α-Reductase deficiency

5α-Reductase deficiency (5-ARD) is an autosomal recessive intersex condition caused by a mutation of the 5α reductase type II gene.

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The list above answers the following questions

Androgen insensitivity syndrome and Mild androgen insensitivity syndrome Comparison

Androgen insensitivity syndrome has 223 relations, while Mild androgen insensitivity syndrome has 71. As they have in common 49, the Jaccard index is 16.67% = 49 / (223 + 71).

References

This article shows the relationship between Androgen insensitivity syndrome and Mild androgen insensitivity syndrome. To access each article from which the information was extracted, please visit:

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