Bardet-Biedl syndrome 11
Bardet-Biedl syndrome that has material basis in mutation in the TRIM32 gene on chromosome 9q33
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Bardet-Biedl syndrome 11
Summary
Bardet-Biedl syndrome 11 is a developmental defect during embryogenesis[1].
Key Facts
- Bardet-Biedl syndrome 11's instance of is recorded as developmental defect during embryogenesis[2].
- Bardet-Biedl syndrome 11's instance of is recorded as rare disease[3].
- Bardet-Biedl syndrome 11's instance of is recorded as class of disease[4].
- Bardet-Biedl syndrome 11 is a type of Bardet-Biedl syndrome[5].
- Bardet-Biedl syndrome 11's health specialty is recorded as medical genetics[6].
- Bardet-Biedl syndrome 11's genetic association is recorded as TRIM32[7].
- Bardet-Biedl syndrome 11's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110133[8].
- Bardet-Biedl syndrome 11's exact match is recorded as http://identifiers.org/doid/DOID:0110133[9].
- Bardet-Biedl syndrome 11's on focus list of Wikimedia project is recorded as WikiProject Medicine[10].