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

* Hereditary diseases

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 connective tissue diseases, especially Ehlers-Danlos Syndrome.

* Genetic diseases: Friedreich's ataxia, Charcot-Marie-Tooth disease, Hereditary neuropathy with liability to pressure palsy

* Hereditary copper metabolic diseases

* inherited or genetic diseases ( Familial Dysautonomia, Hereditary Sensory Autonomic Neuropathy )

** Sub-specialties: Hereditary and genetic eye diseases

Hereditary orthopedic diseases are mainly found in purebred dogs.

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

Hereditary hemorrhagic telangiectasia ( HHT ), also known as Osler-Weber-Rendu disease and Osler-Weber-Rendu syndrome, is a genetic disorder that leads to abnormal blood vessel formation in the skin, mucous membranes, and often in organs such as the lungs, liver and brain.

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.

Other linked genes include the Hereditary Prostate cancer gene 1 ( HPC1 ), the androgen receptor, and the vitamin D receptor.

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.

Examples of genetic tendencies include Protein C deficiency, Protein S deficiency, the Factor V Leiden mutation, Hereditary anti-thrombin deficiency and Prothrombin Mutation G20210A.

The main features of the Tla-o-qui-aht historical socio-political system include: The ‘ fish and fuse ’ annual cycle, and Hereditary structure and social mobility. The fish-and-fuse annual cycle characterizes the historical Tla-o-qui-aht hereditary socio-political system as akin to a watershed management system.

Hereditary causes of sebaceous cysts include Gardner's syndrome and basal cell nevus syndrome.

Isebantu Kyabazinga wa Busoga, the ‎‎ Busoga Lukiiko had expanded to include people other than the Hereditary Rulers.

His titles include Overseer of the Eastern Desert ( he held this position from Year 19 of Amenemhet II until at least Year 6 of Senwosret II ), Hereditary Prince, Count of Menat Khufu, Overseer of priests.

The Hereditary Chiefs or Signatory Heirs of Chief Red Bear and Joseph Montreuil include Jesse Peltier, Donna M. Patenaude, Bradley J. Vervalen, and Carey Decoteau-Peltier Jr.

The couple's only son, Hereditary Prince Alfred, became involved in a scandal involving his mistress and shot himself in January 1899, in the midst of his parents ' twenty-fifth wedding anniversary celebrations.

* 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

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.

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 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.

Hereditary inclusion body myopathy ( IBM ) constitutes a unique group of neuromuscular disorders characterized by adult-onset slowly progressive distal and proximal weakness, and a typical muscle pathology including rimmed vacuoles and filamentous inclusions.

# REDIRECT Hereditary inclusion body myopathy

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.

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

A study found that Hereditary breast-ovarian cancer syndromes ( HBOC ) produce higher than normal levels of breast cancer and ovarian cancer in genetically related families ( either one individual suffered from both, or several individuals in the families suffered from one or the other disease ).

* Dejerine – Sottas disease type of Hereditary motor and sensory neuropathy.

PGD is also now being performed in a disease called Hereditary multiple exostoses ( MHE / MO / HME ).

Hereditary or acquired defects of vWF lead to von Willebrand disease ( vWD ), a bleeding diathesis of the skin and mucous membranes, causing nosebleeds, menorrhagia, and gastrointestinal bleeding.

* Hereditary hemorrhagic telangiectasia or Rendu-Osler-Weber disease

Pes cavus is sometimes — but not always — connected through Hereditary Motor and Sensory Neuropathy Type 1 ( Charcot-Marie-Tooth disease ) and Friedreich's Ataxia ; many other cases of pes cavus are natural.

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

* Hereditary CNS demyelinating disease

The Agent for Foreign Affairs, Van der Goes who had been in favor of distancing the Republic from the French, chose this inopportune moment to secretly approach the King of Prussia as a mediator, with a scheme in which the Hereditary Prince was to become a kind of constitutional monarch in a constitution on the model of the American Constitution.

Hereditary Princess Charlotte ceded her succession rights to her son, Rainier, in 1944, at which time he became Hereditary Prince.

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.

Hereditary relations in metopic synostosis have been found of which 5, 5 % were well defined syndromic.

* 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.

Staffordshire Bull Terriers are known to suffer from Hereditary Cataracts ( HC ) and L-2-hydroxyglutaric aciduria ( L2HGA )— a metabolic disorder resulting in behavioural changes and dementia-like symptoms — both of which are detectable via DNA tests.

He is also, as Lord Abernethy, and in this respect successor to the Gaelic Earls of Fife, the Hereditary Bearer of the Crown of Scotland, a role which the 15th Duke performed at the inauguration of the Scottish Parliament in 1999, as did the 16th Duke at the State Opening of Parliament, 30 June 2011.

Horemheb's specific titles are outlined from his Saqqara tomb which was built while he was still only an official: " Hereditary Prince, Fan-bearer on the Right Side of the King, and Chief Commander of the Army "; the " attendant of the King in his footsteps in the foreign countries of the south and the north "; the " King's Messenger in front of his army to the foreign countries to the south and the north "; and the " Sole Companion, he who is by the feet of his lord on the battlefield on that day of killing Asiatics.

When Tutankhamun died while still a teenager, Horemheb had already been officially designated as the rpat or iry-pat ( basically the " Hereditary or Crown Prince ") and idnw (" Deputy of the King " in the entire land ) by the child pharaoh ; these titles are found inscribed in Horemheb's then private Memphite tomb at Saqqara which dates to the reign of Tutankhamun since the child king's ...

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.

The Commanders organised within the " Russian Grand Priory ", a corporate organisation which existed under various names ; “ Association of Hereditary Commanders ” ( 1928 ), “ Russian Philanthropic Association of the descendants of the hereditary commanders of Sovereign the Order of Malta ” ( 1929 – 1932 ), " Union des Commandeurs Hereditaires et Chevaliers du Grand Prieure Russe de l ' Ordre de St Jean de Jerusalem " ( 1957 – 1958 ) and the longer “ Union ” title given above ( 1958 – 1975 ).

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.

The Commons will occasionally bargain and negotiate with the Lords such as when the Labour Government of 1999 tried to expel all Hereditary Peers from the Lords, and the Lords threatened to wreck the Government's entire legislative agenda and to block every bill which was sent to the chamber.

This led to negotiations between Viscount Cranborne the then Shadow Leader of the House, and the Labour Government which resulted in the Weatherill Amendment to the House of Lords Act 1999 which preserved 92 Hereditary Peers in the house.

He is also the 12th Earl of Bristol, Earl Jermyn of Horningsheath in the County of Suffolk, 13th Baron Hervey of Ickworth in the County of Suffolk, and Hereditary High Steward of the Liberty of St Edmund ( which encompasses the entire ex county of West Suffolk ).

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.

In right of his peerage he became Hereditary High Steward of Ireland, in which capacity he took part in the coronations of Kings Edward VII and George V, and accompanied the former on his state visit to Dublin in July 1903.

The Pioneer Fund supported the distribution of a eugenics film titled Erbkrank (" Hereditary Defective " or " Hereditary Illness ") which was published by the pre-war 1930s Nazi Party.

The earliest such research, Hereditary Genius by Francis Galton ( 1869 ), argued that people vary hugely in “ natural ability ” which is inherited biologically.

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

Hereditary multiple exostoses ( HME or MHE ) is a rare medical condition in which multiple bony spurs or lumps ( also known as exostoses, or osteochondromas ) develop on the bones of a child.