* Type III: Hereditary or acquired.

Hereditary spherocytosis is caused by a variety of molecular defects in the genes that code for spectrin ( alpha and beta ), ankyrin, band 3 protein, protein 4. 2, and other erythrocyte membrane proteins:

Hereditary ( inherited ) hemolytic anemia can be due to membrane defects:

Hereditary ( inherited ) hemolytic anemia can be due to defects in hemoglobin:

Hereditary ( inherited ) hemolytic anemia can be due to enzyme defects:

Already in Norway, the viceroy of Norway, Hereditary Prince Christian Frederik resolved to preserve the integrity of the country, and if possible the union with Denmark, by taking the lead in a Norwegian insurrection.

Hereditary chiefs lead the tribe's communal activities.

Married Hereditary Count Karl Eugen von Neipperg.

Caroline, Princess of Hanover, Hereditary Princess of Monaco ( Caroline Louise Marguerite Grimaldi ; French: princesse de Hanovre, princesse héréditaire de Monaco ; German: Prinzessin von Hannover, Erbprinzessin von Monaco ; born 23 January 1957 ) is the eldest daughter of Rainier III, Prince of Monaco and American actress Grace Kelly, and the elder sister of Albert II, Prince of Monaco, and Princess Stéphanie of Monaco.

Princess Alexandra of Hanover ( German: Alexandra Charlotte Ulrike Maryam Virginia Prinzessin von Hannover ( born 20 July 1999 in Vöcklabruck, Upper Austria ,) is the only child of Ernst August, Prince of Hanover, and Caroline, Hereditary Princess of Monaco.

The remaining members of the House of Mecklenburg-Schwerin are the daughters of Duke Christian Ludwig ; the second son of Frederick Francis IV ; the Duchesses Donata ( born 1956 ) and Edwina ( born 1960 ); Duchess Woizlawa Feodora ( born 1918 ), the daughter of Duke Adolf Friedrich ; and Hereditary Grand Duchess Karin ( née von Schaper ; born 1920 ), the widow of Hereditary Grand Duke Frederick Francis.

** Erich, Hereditary Count von Waldburg zu Zeil und Trauchburg ( born 1962 ).

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.

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.

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.

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 ).

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

* Hereditary hemorrhagic telangiectasia or Rendu-Osler-Weber disease

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.

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 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.

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

* Hereditary CNS demyelinating disease

# Johann ( b. Dresden, 24 August 1498 – d. Dresden, 11 January 1537 ), Hereditary Duke of Saxony ; married on 20 May 1516 to Elizabeth of Hesse.

# Frederick ( b. Dresden, 15 March 1504 – d. Dresden, 26 February 1539 ), Hereditary Duke of Saxony ; married on 27 January 1539 to Elisabeth of Mansfeld.

# Magdalena ( b. Dresden, 7 March 1507 – d. Berlin, 25 January 1534 ), married on 6 November 1524 to Joachim Hector, then Hereditary Elector of Brandenburg.

In 1962 Remey asked his supporters in the United States to organize themselves and elect a " National Spiritual Assembly Under the Hereditary Guardianship " ( NSAUHG ), first elected in 1963.

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.

* Isabella of Savoy ( 1591 – 1626 ), married Alfonso III d ' Este, Hereditary Prince of Modena

* Prince Knud ( 1900 – 1976 ), later Knud, Hereditary Prince of Denmark

* Frederika Luise Wilhelmina ( The Hague, 28 November 1770 – The Hague, 15 October 1819 ), married in The Hague on 14 October 1790 Karl, Hereditary Prince of Braunschweig ( London, 8 February 1766 – Antoinettenruh, 20 September 1806 ), a son of Karl Wilhelm Ferdinand, Duke of Brunswick-Luneburg and Princess Augusta of Great Britain, without issue.

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

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 ).

In Galton's Hereditary Genius ( 1869 ), he examined leadership qualities in the families of powerful men.

" These included, for the Nazis, those suffering from " Congenital Mental Deficiency ", schizophrenia, " Manic-Depressive Insanity ", " Hereditary Epilepsy ", " Hereditary Chorea " ( Huntington ’ s ), Hereditary Blindness, Hereditary Deafness, " any severe hereditary deformity ", as well as " any person suffering from severe alcoholism ".

Injury to the optic nerve can be the result of congenital or inheritable problems like Leber's Hereditary Optic Neuropathy, glaucoma, trauma, toxicity, inflammation, ischemia, infection ( very rarely ), or compression from tumors or aneurysms.

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.