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
Press Enter · cited answer in seconds
0 sources
primary ciliary dyskinesia 21
Summary
primary ciliary dyskinesia 21 is a rare disease[1].
Key Facts
- primary ciliary dyskinesia 21's instance of is recorded as rare disease[2].
- primary ciliary dyskinesia 21's instance of is recorded as class of disease[3].
- primary ciliary dyskinesia 21's subclass of is recorded as primary ciliary dyskinesia[4].
- primary ciliary dyskinesia 21's OMIM ID is recorded as 615294[5].
- primary ciliary dyskinesia 21's Disease Ontology ID is recorded as DOID:0110596[6].
- primary ciliary dyskinesia 21's health specialty is recorded as medical genetics[7].
- primary ciliary dyskinesia 21's genetic association is recorded as DRC1[8].
- primary ciliary dyskinesia 21's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110596[9].
- primary ciliary dyskinesia 21's exact match is recorded as http://identifiers.org/doid/DOID:0110596[10].
- primary ciliary dyskinesia 21's UMLS CUI is recorded as C3809087[11].
- primary ciliary dyskinesia 21's ICD-10-CM is recorded as Q34.8[12].
- primary ciliary dyskinesia 21's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- primary ciliary dyskinesia 21's Mondo ID is recorded as MONDO_0014123[14].
- primary ciliary dyskinesia 21's UniProt disease ID is recorded as DI-03807[15].