Faster access than browser!Similarities between Androgen insensitivity syndrome and Lipoid congenital adrenal hyperplasia
Androgen insensitivity syndrome and Lipoid congenital adrenal hyperplasia have 16 things in common (in Unionpedia): Androgen, Anti-Müllerian hormone, Biosynthesis, Congenital adrenal hyperplasia due to 21-hydroxylase deficiency, Estradiol, Estrogen, Gene, Human penis, Intersex, Leydig cell, Pseudohermaphroditism, Puberty, Secondary sex characteristic, Sex organ, Testosterone, Zygosity.
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.
Androgen and Androgen insensitivity syndrome · Androgen and Lipoid congenital adrenal hyperplasia ·
Anti-Müllerian hormone
Anti-Müllerian hormone (AMH), also known as Müllerian-inhibiting hormone (MIH), is a glycoprotein hormone structurally related to inhibin and activin from the transforming growth factor beta superfamily, whose key roles are in growth differentiation and folliculogenesis.
Androgen insensitivity syndrome and Anti-Müllerian hormone · Anti-Müllerian hormone and Lipoid congenital adrenal hyperplasia ·
Biosynthesis
Biosynthesis (also called anabolism) is a multi-step, enzyme-catalyzed process where substrates are converted into more complex products in living organisms.
Androgen insensitivity syndrome and Biosynthesis · Biosynthesis and Lipoid congenital adrenal hyperplasia ·
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21-OH CAH), in all its forms, accounts for over 95% of diagnosed cases of congenital adrenal hyperplasia, and "CAH" in most contexts refers to 21-hydroxylase deficiency.
Androgen insensitivity syndrome and Congenital adrenal hyperplasia due to 21-hydroxylase deficiency · Congenital adrenal hyperplasia due to 21-hydroxylase deficiency and Lipoid congenital adrenal hyperplasia ·
Estradiol
Estradiol (E2), also spelled oestradiol, is an estrogen steroid hormone and the major female sex hormone.
Androgen insensitivity syndrome and Estradiol · Estradiol and Lipoid congenital adrenal hyperplasia ·
Estrogen
Estrogen, or oestrogen, is the primary female sex hormone.
Androgen insensitivity syndrome and Estrogen · Estrogen and Lipoid congenital adrenal hyperplasia ·
Gene
In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.
Androgen insensitivity syndrome and Gene · Gene and Lipoid congenital adrenal hyperplasia ·
Human penis
The human penis is an external male intromittent organ that additionally serves as the urinal duct.
Androgen insensitivity syndrome and Human penis · Human penis and Lipoid congenital adrenal hyperplasia ·
Intersex
Intersex people are born with any of several variations in sex characteristics including chromosomes, gonads, sex hormones, or genitals that, according to the UN Office of the High Commissioner for Human Rights, "do not fit the typical definitions for male or female bodies".
Androgen insensitivity syndrome and Intersex · Intersex and Lipoid congenital adrenal hyperplasia ·
Leydig cell
Leydig cells, also known as interstitial cells of Leydig, are found adjacent to the seminiferous tubules in the testicle.
Androgen insensitivity syndrome and Leydig cell · Leydig cell and Lipoid congenital adrenal hyperplasia ·
Pseudohermaphroditism
Pseudohermaphroditism, or pseudo-hermaphroditism, is an old clinical term for an organism that is born with primary sex characteristics of one sex but develops the secondary sex characteristics that are different from what would be expected on the basis of the gonadal tissue (ovary or testis).
Androgen insensitivity syndrome and Pseudohermaphroditism · Lipoid congenital adrenal hyperplasia and Pseudohermaphroditism ·
Puberty
Puberty is the process of physical changes through which a child's body matures into an adult body capable of sexual reproduction.
Androgen insensitivity syndrome and Puberty · Lipoid congenital adrenal hyperplasia and Puberty ·
Secondary sex characteristic
Secondary sex characteristics are features that appear during puberty in humans, and at sexual maturity in other animals.
Androgen insensitivity syndrome and Secondary sex characteristic · Lipoid congenital adrenal hyperplasia and Secondary sex characteristic ·
Sex organ
A sex organ (or reproductive organ) is any part of an animal's body that is involved in sexual reproduction.
Androgen insensitivity syndrome and Sex organ · Lipoid congenital adrenal hyperplasia and Sex organ ·
Testosterone
Testosterone is the primary male sex hormone and an anabolic steroid.
Androgen insensitivity syndrome and Testosterone · Lipoid congenital adrenal hyperplasia and Testosterone ·
Zygosity
Zygosity is the degree of similarity of the alleles for a trait in an organism.
Androgen insensitivity syndrome and Zygosity · Lipoid congenital adrenal hyperplasia and Zygosity ·
The list above answers the following questions
- What Androgen insensitivity syndrome and Lipoid congenital adrenal hyperplasia have in common
- What are the similarities between Androgen insensitivity syndrome and Lipoid congenital adrenal hyperplasia
Androgen insensitivity syndrome and Lipoid congenital adrenal hyperplasia Comparison
Androgen insensitivity syndrome has 223 relations, while Lipoid congenital adrenal hyperplasia has 77. As they have in common 16, the Jaccard index is 5.33% = 16 / (223 + 77).
References
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