nemaline myopathy 4
nemaline myopathy that has material basis in heterozygous mutation in the TPM2 gene on chromosome 9p13
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nemaline myopathy 4
Summary
nemaline myopathy 4 is a rare disease[1].
Key Facts
- nemaline myopathy 4's instance of is recorded as rare disease[2].
- nemaline myopathy 4's instance of is recorded as class of disease[3].
- nemaline myopathy 4 is a type of nemaline myopathy[4].
- nemaline myopathy 4 is a type of genetic disease[5].
- nemaline myopathy 4 is a type of autosomal dominant disease[6].
- nemaline myopathy 4's NCI Thesaurus ID is recorded as C164225[7].
- nemaline myopathy 4's genetic association is recorded as TPM2[8].
- nemaline myopathy 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110932[9].
- nemaline myopathy 4's exact match is recorded as http://identifiers.org/doid/DOID:0110932[10].
- nemaline myopathy 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_171881[11].
- nemaline myopathy 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_607[12].
- nemaline myopathy 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].