nemaline myopathy 4
nemaline myopathy that has material basis in heterozygous mutation in the TPM2 gene on chromosome 9p13
Press Enter · cited answer in seconds
0 sources
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's subclass of is recorded as nemaline myopathy[4].
- nemaline myopathy 4's subclass of is recorded as genetic disease[5].
- nemaline myopathy 4's subclass of is recorded as autosomal dominant disease[6].
- nemaline myopathy 4's MeSH descriptor ID is recorded as C538351[7].
- nemaline myopathy 4's OMIM ID is recorded as 609285[8].
- nemaline myopathy 4's OMIM ID is recorded as 609285[9].
- nemaline myopathy 4's Disease Ontology ID is recorded as DOID:0110932[10].
- nemaline myopathy 4's NCI Thesaurus ID is recorded as C164225[11].
- nemaline myopathy 4's genetic association is recorded as TPM2[12].
- nemaline myopathy 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110932[13].
- nemaline myopathy 4's exact match is recorded as http://identifiers.org/doid/DOID:0110932[14].
- nemaline myopathy 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_171881[15].
- nemaline myopathy 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_607[16].
- nemaline myopathy 4's UMLS CUI is recorded as C3807907[17].
- nemaline myopathy 4's UMLS CUI is recorded as C1836447[18].
- nemaline myopathy 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
- nemaline myopathy 4's Mondo ID is recorded as MONDO_0012240[20].
- nemaline myopathy 4's UniProt disease ID is recorded as DI-02035[21].