nemaline myopathy 9
nemaline myopathy characterized by onset in early infancy of muscle weakness with variable severity that has material basis in homozygous or compound heterozygous mutation in the KLHL41 gene on chromosome 2q31
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nemaline myopathy 9
Summary
nemaline myopathy 9 is a rare disease[1]. It is known by 4 alternative names across languages and contexts.[2]
Key Facts
- nemaline myopathy 9's instance of is recorded as rare disease[3].
- nemaline myopathy 9's instance of is recorded as class of disease[4].
- nemaline myopathy 9 is a type of nemaline myopathy[5].
- nemaline myopathy 9 is a type of genetic disease[6].
- nemaline myopathy 9's genetic association is recorded as KLHL41[7].
- nemaline myopathy 9's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110929[8].
- nemaline myopathy 9's exact match is recorded as http://identifiers.org/doid/DOID:0110929[9].
- nemaline myopathy 9's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_607[10].
- nemaline myopathy 9's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
nemaline myopathy 9 is known by 4 alternative names across languages and contexts.[2]