Seckel syndrome 8
Seckel syndrome that has material basis in homozygous mutation in the DNA2 gene on chromosome 10q21
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Seckel syndrome 8
Summary
Seckel syndrome 8 is a rare disease[1].
Key Facts
- Seckel syndrome 8's instance of is recorded as rare disease[2].
- Seckel syndrome 8's instance of is recorded as class of disease[3].
- Seckel syndrome 8's subclass of is recorded as Seckel syndrome[4].
- Seckel syndrome 8's OMIM ID is recorded as 615807[5].
- Seckel syndrome 8's Disease Ontology ID is recorded as DOID:0070009[6].
- Seckel syndrome 8's genetic association is recorded as DNA2[7].
- Seckel syndrome 8's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070009[8].
- Seckel syndrome 8's exact match is recorded as http://identifiers.org/doid/DOID:0070009[9].
- Seckel syndrome 8's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_808[10].
- Seckel syndrome 8's UMLS CUI is recorded as C3891452[11].
- Seckel syndrome 8's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- Seckel syndrome 8's Mondo ID is recorded as MONDO_0014350[13].
- Seckel syndrome 8's UniProt disease ID is recorded as DI-04089[14].