Presentation
Classification level: Disorder Synonym(s): EOMFC Salih myopathy Prevalence: Unknown Inheritance: Autosomal recessive Age of onset: Neonatal, Infancy ICD-10: G71.8 OMIM: 611705 UMLS: C2673677 MeSH: - GARD: - MedDRA: - The documents contained in this web site are presented [orpha.net]
Entire Body System
- Amyloidosis
Storage Disease III AR 100 253 OF 253 ALMS1 Alstrom Syndrome AR 99.92 302 OF 305 ALPK3 Familial Hypertrophic Cardiomyopathy AR 97.29 7 OF 7 ANO5 Miyoshi Muscular Dystrophy, Limb-Girdle Muscular Dystrophy AD,AR 99.78 171 OF 173 APOA1 Familial Visceral Amyloidosis [igenomix.es]
Treatment
The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. [orpha.net]