primary ciliary dyskinesia 5 (Q28024750)
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primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with early onset of a progressive decline in lung function and has material basis in homozygous mutation in the HYDIN gene on chromosome 16q22
- CILD5
- primary ciliary dyskinesia 5 without situs inversus
- CILIARY DYSKINESIA, PRIMARY, 5; CILD5
- CILIARY DYSKINESIA, PRIMARY, 5
- Ciliary Dyskinesia, Primary, type 5
- primary ciliary dyskinesia type 5
- Ciliary Dyskinesia, Primary, 5, Without Situs Inversus
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | primary ciliary dyskinesia 5 |
primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with early onset of a progressive decline in lung function and has material basis in homozygous mutation in the HYDIN gene on chromosome 16q22 |
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