Joubert syndrome 21 (Q32145729)
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Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the CSPP1 gene on chromosome 8q13
- JBTS21
- Joubert Syndrome type 21
- JOUBERT SYNDROME 21; JBTS21
- JOUBERT SYNDROME 21
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Joubert syndrome 21 |
Joubert syndrome that has material basis in homozygous or compound heterozygous mutation in the CSPP1 gene on chromosome 8q13 |
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Statements
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Identifiers
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1 reference