Primary Ciliary Dyskinesia 23
Disease ID: disease_node_14657
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| Dbxref | ICD10CM:Q34.8, MIM:615451 |
|---|---|
| Subclassof | DOID_9562 |
| Data Source | DOID |
| Synonyms | CILD23, primary ciliary dyskinesia 23 with or without situs inversus |
| Doid Label | primary ciliary dyskinesia 23 |
| Doid Description | A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect, respiratory distress and recurrent upper and lower airway infections, and variable occurence of situs inversus and has_material_basis_in homozygous or compound heterozygous mutation in the ARMC4 gene on chromosome 10p. |
| Disease Node Id | disease_node_14657 |
| Doid Id | DOID_0110609 |
| Label | Primary Ciliary Dyskinesia 23 |
- Outgoing r'ship
SUBCLASS_OFto/from Ciliary Motility Disorders(ID:disease_node_2113) (Disease)