Useful english dictionary. 2012.
Werdnig-Hoffman disease — DiseaseDisorder infobox Name = Werdnig Hoffman disease ICD10 = ICD10|G|12|0|g|10 ICD9 = ICD9|335.0 ICDO = Caption = OMIM = 253300 MedlinePlus = 000996 | eMedicineSubj = orthoped eMedicineTopic = 304 DiseasesDB = MeshID = D014897 Werdnig Hoffman… … Wikipedia
Hoffman — August Wilhelm, German chemist, 1818–1892. See Frei Hoffmann reaction, H. violet. Friedrich (Fredericus), German physician, 1660–1742. Professor of Anatomy and Surgery at Halle, noted for clinical observations of a variety of infectious diseases … Medical dictionary
Guido Werdnig — (1844 1919) was a neurologist. [WhoNamedIt|doctor|1713] Werdnig Hoffman disease is named for him.References … Wikipedia
autosomal recessive disease — noun a disease caused by the presence of two recessive mutant genes on an autosome • Syn: ↑autosomal recessive defect • Hypernyms: ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑congenital di … Useful english dictionary
Fazio-Londe disease — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29491 ICD10 = ICD10|G|12|1|g|10 ICD9 = ICD9|335.2 ICDO = OMIM = 211500 MedlinePlus = eMedicineSubj = eMedicineTopic = MeshID = D010244 Fazio Londe disease, also called progressive bulbar… … Wikipedia
nervous system disease — Introduction any of the diseases or disorders that affect the functioning of the human nervous system (nervous system, human). Everything that humans sense, consider, and effect and all the unlearned reflexes of the body depend on the… … Universalium
Spinal Muscular Atrophy Type 2 — (also known as spinal muscular atropy type II ) is an autosomal recessive disease and is a form of spinal muscular atrophy (SMA). Symptoms Children with spinal muscular atrophy type 2 manifest less severe weakness than children with Werdnig… … Wikipedia
List of neurological disorders — This is a list of major and frequently observed neurological disorders (e.g., Alzheimer s disease), symptoms (e.g., back pain), signs (e.g., aphasia) and syndromes (e.g., Aicardi syndrome). Contents: Top · 0–9 A B C D E F G H I J K L M N O P … Wikipedia
Hypotonia — Floppy Muscle Syndrome Classification and external resources ICD 10 P94.2 ICD 9 358 … Wikipedia
autosomal recessive defect — noun a disease caused by the presence of two recessive mutant genes on an autosome • Syn: ↑autosomal recessive disease • Hypernyms: ↑genetic disease, ↑genetic disorder, ↑genetic abnormality, ↑genetic defect, ↑congenital … Useful english dictionary
