primary ciliary dyskinesia 21 (Q28024727)
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primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with a missing Nexin link, infantile onset of chronic sinopulmonary infections, and has material basis in homozygous mutation in the DRC1 gene on chromosome 2p23
- CILD21
- primary ciliary dyskinesia 21 without situs inversus
- Ciliary Dyskinesia, Primary, 21, Without Situs Inversus
- CILIARY DYSKINESIA, PRIMARY, 21; CILD21
- CILIARY DYSKINESIA, PRIMARY, 21
- Ciliary Dyskinesia, Primary, type 21
- primary ciliary dyskinesia type 21
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | primary ciliary dyskinesia 21 |
primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with a missing Nexin link, infantile onset of chronic sinopulmonary infections, and has material basis in homozygous mutation in the DRC1 gene on chromosome 2p23 |
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