Joubert syndrome 9 (Q32145925)
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Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the CC2D2A gene on chromosome 4p15
- JBTS9
- JOUBERT SYNDROME 9; JBTS9
- Joubert Syndrome 9/15, Digenic
- JOUBERT SYNDROME 9
- Joubert Syndrome type 9
Language | Label | Description | Also known as |
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English | Joubert syndrome 9 |
Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the CC2D2A gene on chromosome 4p15 |
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