Reasoning that eminence is caused by genetic traits, he did a study of their heritability, publishing it in 1869 as Hereditary Genius.

Charcot-Marie-Tooth disease ( CMT ), also known as Hereditary Motor and Sensory Neuropathy ( HMSN ), Hereditary Sensorimotor Neuropathy ( HMSN ), or Peroneal Muscular Atrophy, is a heterogeneous inherited disorder of nerves ( neuropathy ) that is characterized by loss of muscle tissue and touch sensation, predominantly in the feet and legs but also in the hands and arms in the advanced stages of disease.

The full inscription read: Iste est gladius Principis et haeredis Boleslai Ducis Poloniae et Masoviae, Lanciciae (" This is a sword of Hereditary Prince Boleslaus, Duke of Poland, Masovia, and Łęczyca ").

Hereditary peerage dignities may be created with writs of summons or by letters patent ; the former method is now obsolete.

That the Bonheur family was renowned as a family of artists is attested to by the fact that Francis Galton, the cousin of Charles Darwin used the Bonheurs as an example of " Hereditary Genius " in his 1869 essay of the same title.

It consists of all cabinet ministers and the Crown Prince or Hereditary Princess when he or she is of age.

He is the Hereditary Grand Duke of Luxembourg, Hereditary Prince of Nassau and holds the title Prince of Bourbon-Parma.

Also known as Hereditary nephritis, it is caused by a nonsense mutation in codon 1027 of the COL4A5 gene on the X chromosome ( glycine to stop codon ), which is similar to Alport's syndrome in humans.

As yet there is no genetic screening test available for Samoyed Hereditary Glomerulopathy.

If there is a male heir apparent, he may be granted the style ' Hereditary Grand Duke '.

The current heir is Hereditary Grand Duke Guillaume.

Of these 92, 1 is the Earl Marshal, a hereditary office always held by the Duke of Norfolk, 1 is the Lord Great Chamberlain, a hereditary office held in gross, currently by the Marquess of Cholmondeley, and the other 90 are elected by other Hereditary Peers.

Hereditary Spastic Paraplegia ( HSP ), also called Familial Spastic Paraplegias or Strumpell-Lorrain disease, is a group of inherited diseases whose main feature is progressive stiffness and contraction ( spasticity ) in the lower limbs, as a result of damage to dysfunction of the nerves.

Hereditary abnormalities of fibrinogen ( the gene is carried on chromosome 4 ) are of both quantitative and qualitative in nature and include afibrinogenaemia, hypofibrinogenaemia, dysfibrinogenaemia, and hypodysfibrinogenaemia.

* Hereditary Spastic Paraplegia-a group of clinically and genetically diverse disorders that share a primary feature, which is the causation of progressive and generally severe lower extremity weakness and spasticity.

Hereditary monarchies most usually arrange succession by a legislated, definite order of succession so that it is well-known beforehand who will be the next monarch.

Hereditary Diffuse Gastric Cancer ( HDGC ) has recently been identified and research is ongoing.

Hereditary met-Hb is caused by a recessive gene.

In Monaco and other monarchies, Caroline is usually referred to and addressed by the female form of the style attributed by tradition to her husband, i. e. Her Royal Highness The Princess of Hanover, rather than by her own legal title ( Her Serene Highness the Hereditary Princess of Monaco ).

Also known as Hereditary Motor and Sensory Neuropathy ( HMSN ), it is genetically heterogeneous and usually presents in the first decade of life with delayed motor milestones, distal muscle weakness, clumsiness and frequent falls.

Hereditary forms are usually autosomal dominant, and instances of autosomal recessive and X-linked inheritance also occur.

Hereditary disorders causing ataxia include autosomal dominant ones such as spinocerebellar ataxia, episodic ataxia, and dentatorubropallidoluysian atrophy, as well as autosomal recessive disorders such as Friedreich's ataxia ( sensory and cerebellar, with the former predominating ) and Niemann Pick disease, ataxia-telangiectasia ( sensory and cerebellar, with the latter predominating ), and abetalipoproteinaemia.

Can occur due to autosomal dominant diseases, such as Hereditary Hemorrhagic Telangiectasia.

Hereditary spherocytosis is a genetically-transmitted ( autosomal dominant ) form of spherocytosis, an auto-hemolytic anemia characterized by the production of red blood cells that are sphere-shaped rather than bi-concave disk shaped ( Donut-Shaped ), and therefore more prone to hemolysis.

Hereditary spherocytosis is an autosomal dominant or recessive trait, most commonly ( though not exclusively ) found in Northern European and Japanese families, although an estimated 25 % of cases are due to spontaneous mutations.

Hereditary haemochromatosis is an autosomal recessive disorder with estimated prevalence in the population of 1 in 500 among patients with European ancestry, with lower incidence in other ethnic groups.

Hereditary hemorrhagic telangiectasia has an autosomal dominant pattern of inheritance.

Hereditary angioedema ( HAE ) exists in three forms, all of which are caused by a genetic mutation that is inherited in an autosomal dominant form.

Lynch syndrome ( HNPCC or Hereditary nonpolyposis colorectal cancer ) is an autosomal dominant genetic condition which has a high risk of colon cancer as well as other cancers including endometrium, ovary, stomach, small intestine, hepatobiliary tract, upper urinary tract, brain, and skin.

* Diffuse nonepidermolytic palmoplantar keratoderma ( also known as " Diffuse orthohyperkeratotic keratoderma ," " Hereditary palmoplantar keratoderma ," " Keratosis extremitatum progrediens ," " Keratosis palmoplantaris diffusa circumscripta ," " Tylosis ," and " Unna-Thost disease ") is inherited as an autosomal dominant condition and is present from infancy, characterized by a well-demarcated, symmetric, often " waxy " keratoderma involving the whole of the palms and soles

* Focal palmoplantar keratoderma with oral mucosal hyperkeratosis ( also known as " Hereditary painful callosity syndrome ," " Keratosis follicularis ," and " Keratosis palmoplantaris nummularis ") is an autosomal dominant keratoderma that represents a clinical overlap syndrome with pachyonychia congenita type I but without the classic nail involvement

Hereditary PSD is an autosomal dominant condition, resulting in a 50 percent chance of passing the disease to offspring.

Hereditary inclusion body myopathies comprise both autosomal recessive and autosomal dominant muscle disorders that have a variable expression ( phenotype ) in individual patients, but all share similar structural features in the muscles.

* Hereditary or congenital sideroblastic anemia may be X-linked or autosomal.

The various individuals who hold fractions of the Lord Great Chamberlainship are technically each Joint Hereditary Lord Great Chamberlain, and the right to exercise the office for a given reign rotates proportionately to the fraction of the office held.

The Hereditary Kingdom of Norway, established by at least three separate genealogical lines of monarchs each allegedly descending from Harald I the Fairhair, was the only realm of medieval Scandinavia which was officially hereditary, not elective.

Hereditary copper accumulation has been described in Bedlington Terriers, where it generally only affects the liver.

Although by 1975, with the death of the secretary, the original leadership had died out and the jurisdiction of the Paris Group came to a definite legal end ; it is asserted that the tradition has been maintained by the Priory of Dacia, ( which was acknowledged as a legal part of the Union ) together with a number of descendants of the Hereditary Commanders associated with the Russian Grand Priory Association.

Ever since Thomas Bruce, 2nd Earl of Ailesbury succeeded his father in 1685, every Earl and Marquess of Ailesbury has also been a Hereditary Warden of Savernake Forest.

Hereditary peerages in other countries may or may not be regulated by the government ; quite often a republic will treat a peerage as a private matter, having no power in the state, and over which the state has no concern.

Since the publication of Francis Galton ’ s Hereditary Genius in 1869, and especially with the accelerated development of intelligence tests in the early 1900s, there has been a vast amount of social scientific research published relative to the question of ‘ greatness ’.

Hereditary angioedema type III has separate pathogenesis, being caused by mutations in F12 gene coding for a serine protease called Factor XII.

From Prince Ernst's previous marriage, she has two half-brothers, Ernst August, Hereditary Prince of Hanover and Prince Christian of Hanover.

A Hereditary werewolf he has the unusual ( for a werewolf ) hobby of marksmanship.

Since losing his seat per the expulsion of the hereditary peers in the House of Lords Act 1999 he has become Co-Chairman of the Hereditary Peerage Association.

This country, the Hereditary Kingdom of Norway, has been the only medieval Scandinavian realm whose kingship was hereditary, not elective.

However, he has not taken an active position on the debate between leadership of Imperial family between his two relatives, Hereditary Prince Imperial Won ( a first cousin and the son of the 9th son of Prince Ui ) and Princess Haewon ( aunt and second eldest daughter of Prince Ui ).

However, he has not taken an active position on the debate over the leadership of the imperial family between his two relatives, Hereditary Prince Imperial Won ( a first cousin and the son of the 9th son of Prince Ui ) and Princess Haewon ( his aunt and second eldest daughter of Prince Ui ).

However, he has not taken an active position on the debate between leadership of Imperial family between his two relatives, Hereditary Prince Imperial Won ( a first cousin and the son of the 9th son of Prince Ui ) and Princess Haewon ( aunt of Prince Won and second eldest daughter of Prince Ui ).

* HRH Hereditary Prince Heinrich Donatus Philipp Umberto of Hesse ( born 17 October 1966 ) married Countess Floria of Faber-Castell in 2003, has a daughter and a son, twins, and a further son.