Joubert syndrome 7 (Q32145897)
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A Joubert syndrome that has material basis in mutation in the RPGRIP1L gene on chromosome 16q12.2.
- JBTS7
- Joubert Syndrome type 7
- JOUBERT SYNDROME 7; JBTS7
- JOUBERT SYNDROME 7
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Joubert syndrome 7 |
A Joubert syndrome that has material basis in mutation in the RPGRIP1L gene on chromosome 16q12.2. |
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Statements
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C159653
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Identifiers
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