Joubert syndrome 10 (Q32145593)
Jump to navigation
Jump to search
A Joubert syndrome that has material basis in X-linked recessive inheritance of mutation in the OFD1 gene on chromosome Xp22.2.
- JBTS10
- Joubert Syndrome type 10
- JOUBERT SYNDROME 10
- JOUBERT SYNDROME 10; JBTS10
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Joubert syndrome 10 |
A Joubert syndrome that has material basis in X-linked recessive inheritance of mutation in the OFD1 gene on chromosome Xp22.2. |
|
Statements
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference