familial isolated hyperparathyroidism
- familial isolated hyperparathyroidism
- familial isolated primary hyperparathyroidism hypoparathyroidism inherited as an autosomal dominant trait in the absence of other inherited endocrinopathies; it is a genetically heterogeneous condition.
Medical dictionary.
2011.
Look at other dictionaries:
familial isolated hyperparathyroidism — FIHP. A rare inherited condition in which one or more tumors form in the parathyroid glands (four pea sized organs found on the thyroid) and cause them to make too much parathyroid hormone. The increased parathyroid hormone causes a loss of… … English dictionary of cancer terms
FIHP — Familial isolated hyperparathyroidism. A rare inherited condition in which one or more tumors form in the parathyroid glands (four pea sized organs found on the thyroid) and cause them to make too much parathyroid hormone. The increased… … English dictionary of cancer terms
CDC73 — Cell division cycle 73, Paf1/RNA polymerase II complex component, homolog (S. cerevisiae), also known as CDC73, is a human gene. [cite web | title = Entrez Gene: CDC73 Cell division cycle 73, Paf1/RNA polymerase II complex component, homolog (S.… … Wikipedia
Hypercalcaemia — Infobox Disease Name = PAGENAME Caption = Calcium DiseasesDB = 6196 ICD10 = ICD10|E|83|5|e|70 ICD9 = ICD9|275.42 ICDO = OMIM = MedlinePlus = 000365 eMedicineSubj = med eMedicineTopic = 1068 eMedicine mult = eMedicine2|emerg|260… … Wikipedia
Multiple endocrine neoplasia — Classification and external resources Micrograph of a medullary thyroid carcinoma, as may be seen in MEN 2A and MEN 2B. H E stain … Wikipedia
Семейный изолированный паратиреоидоз — * сямейны ізаляваны паратырэаідоз * familial isolated hyperparathyroidism редкое наследственное заболевание, при котором одна или больше опухолей образуются на околощитовидных железах и вызывают выработку слишком большого количества… … Генетика. Энциклопедический словарь
List of diseases (H) — A list of diseases in the English wikipedia.DiseasesTOC HaHag Ham* Hageman factor deficiency * Hagemoser Weinstein Bresnick syndrome * Hailey Hailey disease * Hair defect with photosensitivity and mental retardation * Hairy cell leukemia * Hairy… … Wikipedia
Multiple endocrine neoplasia type 2 — MEN type 2A (Sipple syndrome) Classification and external resources Bilateral pheochromocytomas associated with Multiple endocrine neoplasia type 2 ICD 10 D … Wikipedia
Parathyroid hormone — (PTH), or parathormone, is secreted by the parathyroid glands as a polypeptide containing 84 amino acids. It acts to increase the concentration of calcium (Ca2+) in the blood, whereas calcitonin (a hormone produced by the parafollicular cells (C… … Wikipedia
GCM2 — Glial cells missing homolog 2 (Drosophila), also known as GCM2, is a human gene.cite web | title = Entrez Gene: GCM2 glial cells missing homolog 2 (Drosophila)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… … Wikipedia