Joubert syndrome 20 (Q32145716)
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Joubert syndrome that has material basis in compound heterozygous mutation in the TMEM231 gene on chromosome 16q23
- JBTS20
- JOUBERT SYNDROME 20; JBTS20
- Joubert Syndrome type 20
- JOUBERT SYNDROME 20
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Joubert syndrome 20 |
Joubert syndrome that has material basis in compound heterozygous mutation in the TMEM231 gene on chromosome 16q23 |
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Statements
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Identifiers
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1 reference