:* 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-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.

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 ).

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.

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.

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.

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

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 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.

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.

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 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.

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

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

The traditional official title, used until 1980, for other dynastic male heirs was Hereditary Prince of Sweden (), although the word prince () was used in constitutional legal texts such as the Instrument of Government of 1809 and also colloquially and informally.

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 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.

At such time, he would receive the traditional titles of the heir-apparent to Monaco's throne, becoming HSH Hereditary Prince Andrea of Monaco, Marquis of Baux.

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.

Several territories of the Empire were not represented, while some officials ( such as the Hereditary Usher ) were non-voting members ; neither qualified as Imperial States.

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

The ruling or noble class of the Brigade ( referred to as " brazazz " or " brass ass ") bear titles that refer to the Brigade's former military organization based on officer ranks, such as " Hereditary Captain " or " Hereditary Colonel.

Christian ( 1818 – 1906 ), who in the 1840's became Hereditary Prince of Denmark ( though his brothers did not become such ) and in 1863 became King Christian IX of Denmark.

The titles of heirs apparent to a monarchy are treated as substantive titles, such as the Dutch Prince of Orange, Belgian Duke of Brabant, Spanish Prince of Asturias, British Prince of Wales, Danish Crown Prince, Luxemburgish Hereditary Grand Duke, and the Monégasque and Liechtensteiner Hereditary Princes.