nephronophthisis 12 (Q32147433)
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nephronophthisis that has material basis in homozygous or compound heterozygous mutation in the TTC21B gene on chromosome 2q24
- NPHP12
- NEPHRONOPHTHISIS 12; NPHP12
- Nephronophthisis type 12
- Joubert Syndrome 11
- NEPHRONOPHTHISIS 12
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | nephronophthisis 12 |
nephronophthisis that has material basis in homozygous or compound heterozygous mutation in the TTC21B gene on chromosome 2q24 |
|
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