Mohr syndrome — (mor) [Otto Lous Mohr, Norwegian geneticist, 1886–1967] see under syndrome … Medical dictionary
Mohr–Tranebjærg syndrome — Classification and external resources OMIM 304700 Mohr–Tranebjærg syndrome (MTS) is a rare X liked recessive syndrome also known as Deafness dystonia syndrome and caused by mutation in the TIMM8A gene. It was first described in 1960 … Wikipedia
Syndrome de mohr-tranebjaerg — Autre nom Syndrome surdité dystonie neuropathie optique Référence MIM … Wikipédia en Français
Syndrome de Mohr-Tranebjaerg — Référence MIM 304700 Transmission Récessive liée à l X Chromosome Xq22 Gène TIMM8A Empreinte parentale Non … Wikipédia en Français
Syndrome dépressif — Dépression (psychiatrie) Pour les articles homonymes, voir Dépression. Las de la vie Peinture de Ferdinand Hodler (18 … Wikipédia en Français
syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… … Medical dictionary
Jan Mohr — Jan Gunnar Faye Mohr, Norwegian Danish physician and geneticist. Known for his discovery of the first cases of autosomal genetic linkage in man, between the Lutheran blood groups and the ABH secretor system, and between these and the hereditary… … Wikipedia
Orofaciodigital syndrome 1 — Classification and external resources OMIM 311200 DiseasesDB 29898 MeSH … Wikipedia
Orofaciodigital syndrome — type I (OFD1) is an X linked disorder characterized by malformations of the face, oral cavity, and digits with polycystic kidney disease and variable involvement of the central nervous system. cite journal author=Badano JL, Mitsuma N, Beales PL,… … Wikipedia
oral-facial-digital syndrome type II — Mohr s … Medical dictionary