3MC syndrome 2
3MC syndrome that has material basis in homozygous mutation in the COLEC11 gene on chromosome 2p25
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3MC syndrome 2
Summary
3MC syndrome 2 is a class of disease[1].
Key Facts
- 3MC syndrome 2's instance of is recorded as class of disease[2].
- 3MC syndrome 2's subclass of is recorded as 3MC syndrome[3].
- 3MC syndrome 2's MeSH descriptor ID is recorded as C535586[4].
- 3MC syndrome 2's OMIM ID is recorded as 265050[5].
- 3MC syndrome 2's Disease Ontology ID is recorded as DOID:0060576[6].
- 3MC syndrome 2's Orphanet ID is recorded as 2998[7].
- 3MC syndrome 2's genetic association is recorded as COLEC11[8].
- 3MC syndrome 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060576[9].
- 3MC syndrome 2's exact match is recorded as http://identifiers.org/doid/DOID:0060576[10].
- 3MC syndrome 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
- 3MC syndrome 2's Mondo ID is recorded as MONDO_0009927[12].
- 3MC syndrome 2's UniProt disease ID is recorded as DI-03130[13].
- 3MC syndrome 2's Experimental Factor Ontology ID is recorded as 1001977[14].