Seckel syndrome 6
Seckel syndrome that has material basis in homozygous mutation in the CEP63 gene on chromosome 3q22
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Seckel syndrome 6
Summary
Seckel syndrome 6 is a developmental defect during embryogenesis[1]. It is known by 4 alternative names across languages and contexts.[2]
Key Facts
- Seckel syndrome 6's instance of is recorded as developmental defect during embryogenesis[3].
- Seckel syndrome 6's instance of is recorded as rare disease[4].
- Seckel syndrome 6's instance of is recorded as class of disease[5].
- Seckel syndrome 6 is a type of Seckel syndrome[6].
- Seckel syndrome 6's genetic association is recorded as CEP63[7].
- Seckel syndrome 6's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070006[8].
- Seckel syndrome 6's exact match is recorded as http://identifiers.org/doid/DOID:0070006[9].
- Seckel syndrome 6's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].
Why It Matters
Seckel syndrome 6 is known by 4 alternative names across languages and contexts.[2]