Meckel syndrome 6
Meckel syndrome that has material basis in an autosomal recessive mutation of CC2D2A on chromosome 4p15.32
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Meckel syndrome 6
Summary
Meckel syndrome 6 is a rare disease[1].
Key Facts
- Meckel syndrome 6's instance of is recorded as rare disease[2].
- Meckel syndrome 6's instance of is recorded as class of disease[3].
- Meckel syndrome 6's subclass of is recorded as Meckel syndrome[4].
- Meckel syndrome 6's MeSH descriptor ID is recorded as C567365[5].
- Meckel syndrome 6's OMIM ID is recorded as 612284[6].
- Meckel syndrome 6's Disease Ontology ID is recorded as DOID:0070120[7].
- Meckel syndrome 6's genetic association is recorded as CC2D2A[8].
- Meckel syndrome 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070120[9].
- Meckel syndrome 6's exact match is recorded as http://identifiers.org/doid/DOID:0070120[10].
- Meckel syndrome 6's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_564[11].
- Meckel syndrome 6's UMLS CUI is recorded as C2676790[12].
- Meckel syndrome 6's ICD-10-CM is recorded as Q61.9[13].
- Meckel syndrome 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- Meckel syndrome 6's Mondo ID is recorded as MONDO_0012848[15].
- Meckel syndrome 6's UniProt disease ID is recorded as DI-00704[16].