primary ciliary dyskinesia 33
primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with recurrent upper and lower respiratory infections and has material basis in homozygous mutation in the GAS8 gene on chromosome 16q24
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primary ciliary dyskinesia 33
Summary
primary ciliary dyskinesia 33 is a rare disease[1].
Key Facts
- primary ciliary dyskinesia 33's instance of is recorded as rare disease[2].
- primary ciliary dyskinesia 33's instance of is recorded as class of disease[3].
- primary ciliary dyskinesia 33's subclass of is recorded as primary ciliary dyskinesia[4].
- primary ciliary dyskinesia 33's OMIM ID is recorded as 616726[5].
- primary ciliary dyskinesia 33's Disease Ontology ID is recorded as DOID:0110619[6].
- primary ciliary dyskinesia 33's health specialty is recorded as medical genetics[7].
- primary ciliary dyskinesia 33's genetic association is recorded as GAS8[8].
- primary ciliary dyskinesia 33's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110619[9].
- primary ciliary dyskinesia 33's exact match is recorded as http://identifiers.org/doid/DOID:0110619[10].
- primary ciliary dyskinesia 33's UMLS CUI is recorded as C4225230[11].
- primary ciliary dyskinesia 33's ICD-10-CM is recorded as Q34.8[12].
- primary ciliary dyskinesia 33's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- primary ciliary dyskinesia 33's Mondo ID is recorded as MONDO_0014750[14].
- primary ciliary dyskinesia 33's UniProt disease ID is recorded as DI-04621[15].