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

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

* 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 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.

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.

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 ).

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 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.

Hereditary met-Hb is caused by a recessive gene.

roa-rup: Hereditary methemoglobinemia ( recessive )

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.

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.

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

Honorary Style, Professional Rank, Royal Hereditary Title, Federal Title, State Title, Non-royal Hereditary Title, Doctor ( of medicine or philosophy ), Haji / Hajjah ( for Muslim men and women who have performed the Hajj ), Name.

While the title of Hereditary Lay Abbot was a feudal position that was often exercised in name only, Crinán does seem to have acted as Abbot in charge of the monastery in his time.

Hereditary Werewolves acquire these enhanced abilities gradually, following puberty, and have their first change in their late teens or early 20s.

These provinces, together, became known as the Habsburg Hereditary Lands, although they were sometimes all lumped together simply as Austria.

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 ).

It consists of all cabinet ministers and the Crown Prince or Hereditary Princess when he or she is of age.

Ahmose is identified with an impressive array of titles: Hereditary Princess ( iryt-p ` t ), Great of Praises ( wrt-hzwt ), Mistress of Great Beloved Sweetness ( nebt-bnrt -‘ 3 ( t )- mrwt ), Great King ’ s Wife, his beloved ( hmt-niswt-wrt meryt. f ), Mistress of Gladness ( hnwt-ndjm-ib ), Lady of all Women ( hnwt-hmwt-nbwt ), Mistress of the Two Lands ( hnwt-t3wy ), Companion of Horus ( zm3yt-hrw ), Beloved Companion of Horus ( zm3yt-hrw-mryt. f ), King ’ s Sister ( snt-niswt )

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.

As his father's chosen successor the Prince employed three distinctive titles: " Hereditary Prince ", " Royal scribe " and " Generalissimo "; the latter two of his titles are mentioned in a text at Amenhotep III's temple at Soleb and all three royal titles appear on a lintel now in Florence, Italy.

The Napoleonic Wars caused disruptions where many parts of the Hereditary lands were lost, but all these, along with the former Archbishopric of Salzburg, which had previously been temporarily annexed between 1805 and 1809, were recovered at the peace in 1815, with the exception of the Vorlande.

Until the mid 17th century, all of the provinces were not even necessarily ruled by the same person-junior members of the family often ruled portions of the Hereditary Lands as private apanages.

Hereditary Khan of the Kharoti ( Ghilzai ), he became head of the Spinzar Cotton Company with factories all over Afghanistan, building houses, clubs and hotels under the Spinzar brand.

Like the Reigning Prince and all other members of the Princely Family, the Hereditary Prince is styled His ( Her ) Serene Highness.