hereditary proximal myopathy with early respiratory failure

Summary

hereditary proximal myopathy with early respiratory failure is a rare disease^[1].

Key Facts

• hereditary proximal myopathy with early respiratory failure's instance of is recorded as rare disease^[2].
• hereditary proximal myopathy with early respiratory failure's instance of is recorded as class of disease^[3].
• hereditary proximal myopathy with early respiratory failure's subclass of is recorded as progressive muscular dystrophy^[4].
• hereditary proximal myopathy with early respiratory failure's subclass of is recorded as inclusion myopathy^[5].
• hereditary proximal myopathy with early respiratory failure's subclass of is recorded as qualitative or quantitative defects of titin^[6].
• hereditary proximal myopathy with early respiratory failure's subclass of is recorded as myofibrillar myopathy^[7].
• hereditary proximal myopathy with early respiratory failure's MeSH descriptor ID is recorded as C566343^[8].
• hereditary proximal myopathy with early respiratory failure's OMIM ID is recorded as 603689^[9].
• hereditary proximal myopathy with early respiratory failure's Disease Ontology ID is recorded as DOID:0111188^[10].
• hereditary proximal myopathy with early respiratory failure's Orphanet ID is recorded as 178464^[11].
• hereditary proximal myopathy with early respiratory failure's genetic association is recorded as TTN^[12].
• hereditary proximal myopathy with early respiratory failure's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_178464^[13].
• hereditary proximal myopathy with early respiratory failure's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111188^[14].
• hereditary proximal myopathy with early respiratory failure's exact match is recorded as http://identifiers.org/doid/DOID:0111188^[15].
• hereditary proximal myopathy with early respiratory failure's UMLS CUI is recorded as C1863599^[16].
• hereditary proximal myopathy with early respiratory failure's ICD-10-CM is recorded as G71.0^[17].
• hereditary proximal myopathy with early respiratory failure's PatientsLikeMe condition ID is recorded as hmerf^[18].
• hereditary proximal myopathy with early respiratory failure's GARD rare disease ID is recorded as 12591^[19].
• hereditary proximal myopathy with early respiratory failure's on focus list of Wikimedia project is recorded as WikiProject Medicine^[20].
• hereditary proximal myopathy with early respiratory failure's Mondo ID is recorded as MONDO_0011362^[21].
• hereditary proximal myopathy with early respiratory failure's UniProt disease ID is recorded as DI-01727^[22].