Seckel syndrome 9
Seckel syndrome that has material basis in homozygous mutation in the TRAIP gene on chromosome 3p21
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Seckel syndrome 9
Summary
Seckel syndrome 9 is a developmental defect during embryogenesis[1]. It is known by 3 alternative names across languages and contexts.[2]
Key Facts
- Seckel syndrome 9's instance of is recorded as developmental defect during embryogenesis[3].
- Seckel syndrome 9's instance of is recorded as rare disease[4].
- Seckel syndrome 9's instance of is recorded as class of disease[5].
- Seckel syndrome 9 is a type of Seckel syndrome[6].
- Seckel syndrome 9's genetic association is recorded as TRAIP[7].
- Seckel syndrome 9's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070005[8].
- Seckel syndrome 9's exact match is recorded as http://identifiers.org/doid/DOID:0070005[9].
- Seckel syndrome 9's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
Why It Matters
Seckel syndrome 9 is known by 3 alternative names across languages and contexts.[2]