marie's ataxia
111Barraquer–Simons syndrome — Barraquer Simons syndrome Classification and external resources ICD 10 272.6 OMIM 608709 DiseasesDB …
112Naegeli–Franceschetti–Jadassohn syndrome — Classification and external resources OMIM 161000 DiseasesDB 29767 eMedicine …
113Congenital contractural arachnodactyly — Beals syndrome Classification and external resources OMIM 121050 DiseasesDB 29326 Beals syndrome (Congenital contractural arachnodactyl …
114Freeman–Sheldon syndrome — Freeman Sheldon syndrome Classification and external resources ICD 9 759.89 …
115Reticular pigmented anomaly of the flexures — Classification and external resources OMIM 179850 Reticular pigmented anomaly of the flexures (also known as Dark dot disease, and Dowling–Degos disease ) is a reticular pigmented anomaly of the flexures, an autosomal dominant pigmentary disorder …
116Buschke–Ollendorff syndrome — Buschke Ollendorff syndrome Classification and external resources OMIM 166700 DiseasesDB 30071 Buschke–Ollendorff syndrome, also known as Dermatofibrosis lenticularis diss …
117Desmin-related myofibrillar myopathy — Classification and external resources OMIM 601419 Desmin related myofibrillar myopathy is a subgroup of the myofibrillar myopathy diseases and is the result of a mutation in the gene that codes for desmin which prevents it from forming protein… …
118Naxos syndrome — Classification and external resources Cutaneous phenotype of Naxos disease: woolly hair (A), palmar (B) and plantar (C) keratoses. OMIM …
119May-Hegglin anomaly — Classification and external resources ICD 10 D72.0 …
120Dunnigan familial partial lipodystrophy — Classification and external resources OMIM 151660 Dunnigan type familial partial lipodystrophy, abbreviated as (FPLD), is a rare monogenic form of insulin resistance characterized by loss of subcutaneous fat from the extremities, trunk, and… …
