syndrome de duchenne
21Orofaciodigital syndrome 1 — Classification and external resources OMIM 311200 DiseasesDB 29898 MeSH …
22Nasodigitoacoustic syndrome — Classification and external resources ICD 10 Q …
23FG syndrome — Classification and external resources OMIM 305450 DiseasesDB 32162 GeneReviews …
24MASA syndrome — Classification and external resources OMIM 303350 MASA syndrome, also called CRASH syndrome and Gareis Mason syndrome,[1] is a rare X linked recessive[2 …
25Oculocerebrorenal syndrome — Classification and external resources ICD 10 E72.0 ICD 9 270.8 …
26McLeod syndrome — This article is about the genetic disease of the blood, not MacLeod s syndrome (the lung disease). McLeod syndrome Classification and external resources OMIM 314850 DiseasesDB 29708 …
27Craniofrontonasal syndrome — Classification and external resources OMIM 304110 Craniofrontonasal syndrome is an X linked syndrome which is more severe in females than males. Often males will have only hypertelorism (far apart eyes), whereas females have frontonasal dysplasia …
28CHILD syndrome — For other uses, see Child (disambiguation). CHILD syndrome Classification and external resources OMIM 308050 DiseasesDB 34609 Con …
29Mohr–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 …
30Simpson–Golabi–Behmel syndrome — Classification and external resources X linked recessive inheritance. ICD 10 Q …
