Joubert syndrome 9 (Q32145925)
Jump to navigation
Jump to search
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 |
|---|---|---|---|
| English | Joubert syndrome 9 |
Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the CC2D2A gene on chromosome 4p15 |
|
Statements
2 references
3 references
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference