Seckel syndrome 7
Seckel syndrome that has material basis in compound heterozygous mutation in the NIN gene on chromosome 14q22
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Seckel syndrome 7
Summary
Seckel syndrome 7 is a developmental defect during embryogenesis[1]. It is known by 5 alternative names across languages and contexts.[2]
Key Facts
- Seckel syndrome 7's instance of is recorded as developmental defect during embryogenesis[3].
- Seckel syndrome 7's instance of is recorded as rare disease[4].
- Seckel syndrome 7's instance of is recorded as class of disease[5].
- Seckel syndrome 7 is a type of Seckel syndrome[6].
- Seckel syndrome 7's genetic association is recorded as NIN[7].
- Seckel syndrome 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070011[8].
- Seckel syndrome 7's exact match is recorded as http://identifiers.org/doid/DOID:0070011[9].
- Seckel syndrome 7's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_319675[10].
- Seckel syndrome 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].
Why It Matters
Seckel syndrome 7 is known by 5 alternative names across languages and contexts.[2]