Hereditary
31Hereditary coproporphyria — Classification and external resources Coproporphyrinogen III ICD 10 E …
32Hereditary title — Hereditary titles, in a general sense, are titles, positions or styles that are hereditary and thus tend or are bound to remain in particular families. Some hereditary titles are inherited only by the eldest son (see primogeniture) [cite web|… …
33Hereditary mucoepithelial dysplasia — Classification and external resources ICD 10 L98.9 ICD 9 709.9 …
34Hereditary inclusion body myopathy — Hereditary inclusion body myopathies (HIBM) are a heterogeneous group of genetic disorders which have different symptoms. Generally, they are neuromuscular disorders characterized by muscle weakness developing in young adults. Hereditary… …
35Hereditary equine regional dermal asthenia — (HERDA) aka hyperelastosis cutis (HC) is an inherited autosomal recessive connective tissue disorder. It develops from a homozygous recessive mutation that weakens collagen fibers that allow the skin of the animal to stay connected to the rest of …
36Hereditary Neuralgic Amyotrophy — Hereditary Neuralgic Amyotropy, alternatively referred to as HNA, is a neuralgic disorder that is characterized by nerve damage and muscle atrophy, preceded by severe pain. It is caused by a mutation to the gene locus 17 q25 of the septin 9 gene …
37Hereditary cancer — Hereditary cancers happen when a person is born with a mutation or change in a single copy of a protective gene pair. The term “hereditary cancer syndrome” describes an inherited gene mutation that increases the chance to develop one or more… …
38hereditary peer — UK US noun [countable] [singular hereditary peer plural hereditary peers] someone who has become a member of the British house of lords because their parent was a member Thesaurus: in the uk parliament and assemblies …
39Hereditary President — is the top ranking government official in the executive branch of the People s Republic of Haven, a fictional place in the Honorverse. As the name implies the position was hereditary, although the order of succession is unknown. All hereditary… …
40Hereditary persistence of fetal hemoglobin — (HPFH, BrE: Hereditary persistence of foetal haemoglobin ) is a benign condition in which significant fetal hemoglobin (hemoglobin F) production continues well into adulthood, disregarding the normal shutoff point after which only adult type… …
