Hereditary inclusion body myopathies ( HIBM ) are a heterogeneous group of genetic disorders which have different symptoms.

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.

# REDIRECT Hereditary inclusion body myopathy

* Hereditary diseases that cause damage to the liver include hemochromatosis, involving accumulation of iron in the body, and Wilson's disease, which causes the body to retain copper.

Gitxsan Nation is one of Canada's First Nations and is a name used when referring to the Office of the Hereditary Chiefs of the Gitxsan, which is the formal governing body of the Gitxsan people.

* Mindjedef-" King ’ s son of his body ", " Hereditary prince ", " Treasurer of the King of Lower Egypt ", etc.

The Office of the Hereditary Chiefs is the main political body of the Wet ' suwet ' en and is involved in the negotiating process for an eventual treaty with the British Columbia government.

::* Hereditary internal sphincter myopathy

Due to the heavy influx of American Quarter Horse breeding, some Paints may also carry genetic disorders such as Hyperkalemic Periodic Paralysis ( HYPP ), Hereditary Equine Regional Dermal Asthenia ( HERDA ), Equine polysaccharide storage myopathy ( called PSSM-polysaccharide storage myopathy-in Paints, Quarter Horses and Appaloosas ), Malignant hyperthermia ( MH ) and Glycogen Branching Enzyme Deficiency ( GBED ).

:* The Hereditary spherocytosis ( HS ) syndromes are a group of inherited disorders characterized by the presence of spherical-shaped erythrocytes on the peripheral blood smear.

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 spastic paraplegia-a group of inherited disorders that are characterized by progressive weakness and stiffness of the legs

* 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.

On 24 June 1928, a group of 12 Russian Hereditary Commanders met in Paris to re-establish the activities of the Russian Grand Priory.

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.

Hereditary disorders of all PPARs have been described, generally leading to a loss in function and concomitant lipodystrophy, insulin resistance, and / or acanthosis nigricans.

Hereditary genetic disorders such as neurofibromatoses ( type 1 and type 2 ) and tuberous sclerosis complex are known to predispose to their development.

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.

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 haemochromatosis is characterized by an accelerated rate of intestinal iron absorption and progressive iron deposition in various tissues that typically begins to be expressed in the third to fifth decades of life, but may occur in children.

Hereditary angioedema ( types I and II ) ( also known as " Quincke edema " after discoverer Heinrich Quincke ) presents in the second to fourth decade, and is characterized by local swelling in subcutaneous tissues.

* 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

His services were rewarded in 1498 when Maximilian bestowed upon him the title of Hereditary Governor ( potestat ) of Friesland, but he had to make good his claim by force of arms.

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

The genetic basis of HD was discovered in 1993 by an international collaborative effort spearheaded by the Hereditary Disease Foundation.

Wilhelm, Duke of Urach ( 1864 – 1928 ), had the distinction of being under consideration for five thrones at different times: that of King of Wurttemberg in the 1890s, as the senior agnate by primogeniture when it became likely that King William II would die without male descendants, leaving as heir Duke Albrecht of Wurttemberg, a more distantly related, albeit dynastic, royal kinsman ; Prince of Albania in 1913 ; Prince of Monaco as the next heir by proximity of blood following the Hereditary Prince Louis during a succession crisis resolved in July 1918 ; Grand Duke of Alsace-Lorraine in 1917, and his election by the Taryba as King of Lithuania in July 1918.

In the ensuing political vacuum a triumvirate of former Orangist regents, led by Gijsbert Karel van Hogendorp, invited the former Hereditary Prince ( the old Stadtholder had died in 1806 ) to assume power as " Sovereign Prince.

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

Hereditary peerage was re-established to Louis's behest by the ministry.

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.

Upon the 1278 Battle on the Marchfeld the colours were assumed by the victorious House of Habsburg and gradually became the coat of arms of the dynasty's Hereditary Lands within the Habsburg Monarchy.

Samoyeds can be affected by a genetic disease known as " Samoyed Hereditary Glomerulopathy ", a renal disease.

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.

Prince Edward was baptised on 30 November 1767 ; his godparents were The Hereditary Prince of Brunswick-Lüneburg ( his paternal uncle by marriage, for whom The Earl of Hertford, Lord Chamberlain, stood proxy ), Duke Charles of Mecklenburg-Strelitz ( his maternal uncle, for whom The Earl of Huntingdon, Groom of the Stole, stood proxy ), The Hereditary Princess of Brunswick-Wolfenbüttel ( his paternal aunt, who was represented by a proxy ) and The Landgravine of Hesse-Kassel ( his twice-paternal great-aunt, for whom The Duchess of Argyll, Lady of the Bedchamber to The Queen, stood proxy ).

A two-volume work, Foundations of Human Hereditary Teaching and Racial Hygiene, co-written by him, Erwin Baur and Fritz Lenz, served as the " scientific " basis for Nazism's attitude toward other races.

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.

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.

Nefertiti had many titles including Hereditary Princess ( iryt-p ` t ); Great of Praises ( wrt-hzwt ); Lady of Grace ( nbt-im3t ), Sweet of Love ( bnrt-mrwt ); Lady of The Two Lands ( nbt-t3wy ); Main King ’ s Wife, his beloved ( hmt-niswt -‘ 3t meryt. f ); Great King ’ s Wife, his beloved ( hmt-niswt-wrt meryt. f ), Lady of all Women ( hnwt-hmwt-nbwt ); and Mistress of Upper and Lower Egypt ( hnwt-Shm ’ w-mhw ).

Pichel avoided the problems of being an imitation of " SMOM " by giving his organization a mythical history by claiming the American organization he led was founded by Russian Hereditary Commanders living in, or visiting, the USA and dated to 1908 ; a spurious claim, but which nevertheless misled many including some academics.

A special case was Empress Maria Theresa ; she bore the imperial title as the wife of Francis I, Holy Roman Emperor, but she herself was the monarch of the Austrian Hereditary Lands including Bohemia and Hungary.

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.