nemaline myopathy 6
human disease
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nemaline myopathy 6
Summary
nemaline myopathy 6 is a rare disease[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- nemaline myopathy 6's instance of is recorded as rare disease[3].
- nemaline myopathy 6's instance of is recorded as class of disease[4].
- nemaline myopathy 6 is a type of nemaline myopathy[5].
- nemaline myopathy 6 is a type of genetic disease[6].
- nemaline myopathy 6 is a type of autosomal dominant disease[7].
- nemaline myopathy 6's genetic association is recorded as KBTBD13[8].
- nemaline myopathy 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110935[9].
- nemaline myopathy 6's exact match is recorded as http://identifiers.org/doid/DOID:0110935[10].
- nemaline myopathy 6's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_607[11].
- nemaline myopathy 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
nemaline myopathy 6 is known by 5 alternative names across languages and contexts.[2]