Hereditary forms of diabetes insipidus account for less than 10 % of the cases of diabetes insipidus seen in clinical practice.

* Hereditary forms, often together with a sensory neuropathy ( hereditary sensory and autonomic neuropathy, five types )

Hereditary forms of ovarian cancer can be caused by mutations in specific genes ( most notably BRCA1 and BRCA2, but also in genes for hereditary nonpolyposis colorectal cancer ).

Hereditary aniridia is usually transmitted in an autosomal dominant manner ( each offspring has a 50 % chance of being affected ), although rare autosomal recessive forms ( such as Gillespie syndrome ) have also been reported.

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

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

The male-line descendants of Grand Duchess Charlotte who are the children of a reigning Grand Duke or The Hereditary Grand Duke hold the titles Prince ( ss ) of Luxembourg and Prince ( ss ) of Nassau with the style of His / Her Royal Highness.

Male line descendants of Grand Duchess Charlotte who are not the children of a Grand Duke or Hereditary Grand Duke are Prince ( ss ) of Nassau with the style of His / Her Royal Highness ( coming from their status as male-line descendants of Duke Robert of Parma ).

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 paraplegias are classified based on the symptoms ; on their mode of inheritance ; on the patient ’ s age at onset ; and, ultimately, on the gene associated with the condition.

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 inherited disorders that are characterized by progressive weakness and stiffness of the legs

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.

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.

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 ...

The children are, respectively, second, fourth and third in the line of succession to the Monegasque throne, after their mother, HRH the Princess of Hanover, Hereditary Princess of Monaco.

Included are traditional stories about creation and other phenomena told by Aboriginal people such as Mi ' kmaq Hereditary Chief Stephen Augustine who recounts the beginning of the world in the Creation Stories Theatre film.

The Marquesses are also Hereditary Constables of Hillsborough Fort.

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 supporters are normally limited to hereditary peers, certain members of the Royal Family, chiefs of Scottish Clans, Scottish feudal barons whose baronies predate 1587.

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

Among his 29 titles are: Master of the Royal Household of Scotland and Hereditary Keeper of the Great Seal of Scotland ( ranking 25th in the Scottish Order of Precedence ), Admiral of the Western Coasts and Isles, and the Chief of Clan Campbell.

The Hereditary Chiefs who are leading Tla-o-qui-aht through this process are:

There is currently a standing agreement that decisions regarding resource use are done through consensus of the six Hereditary Chiefs.

Currently, regionally focused appointments are made by the Hereditary Chiefs.

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.

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 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 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.

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.

Hereditary met-Hb is caused by a recessive gene.

roa-rup: Hereditary methemoglobinemia ( recessive )