myofibrillar myopathy 8
human disease
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myofibrillar myopathy 8
Summary
myofibrillar myopathy 8 is a rare disease[1].
Key Facts
- myofibrillar myopathy 8's instance of is recorded as rare disease[2].
- myofibrillar myopathy 8's instance of is recorded as class of disease[3].
- myofibrillar myopathy 8's subclass of is recorded as myofibrillar myopathy[4].
- myofibrillar myopathy 8's subclass of is recorded as autosomal recessive disease[5].
- myofibrillar myopathy 8's OMIM ID is recorded as 617258[6].
- myofibrillar myopathy 8's Disease Ontology ID is recorded as DOID:0080308[7].
- myofibrillar myopathy 8's genetic association is recorded as PYROXD1[8].
- myofibrillar myopathy 8's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080308[9].
- myofibrillar myopathy 8's exact match is recorded as http://identifiers.org/doid/DOID:0080308[10].
- myofibrillar myopathy 8's UMLS CUI is recorded as C4310645[11].
- myofibrillar myopathy 8's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- myofibrillar myopathy 8's Mondo ID is recorded as MONDO_0014993[13].
- myofibrillar myopathy 8's UniProt disease ID is recorded as DI-04890[14].