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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primary ciliary dyskinesia 5
Summary
primary ciliary dyskinesia 5 is a rare disease[1].
Key Facts
- primary ciliary dyskinesia 5's instance of is recorded as rare disease[2].
- primary ciliary dyskinesia 5's instance of is recorded as class of disease[3].
- primary ciliary dyskinesia 5's subclass of is recorded as primary ciliary dyskinesia[4].
- primary ciliary dyskinesia 5's MeSH descriptor ID is recorded as C563886[5].
- primary ciliary dyskinesia 5's OMIM ID is recorded as 608647[6].
- primary ciliary dyskinesia 5's Disease Ontology ID is recorded as DOID:0110617[7].
- primary ciliary dyskinesia 5's health specialty is recorded as medical genetics[8].
- primary ciliary dyskinesia 5's genetic association is recorded as HYDIN[9].
- primary ciliary dyskinesia 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110617[10].
- primary ciliary dyskinesia 5's exact match is recorded as http://identifiers.org/doid/DOID:0110617[11].
- primary ciliary dyskinesia 5's UMLS CUI is recorded as C1837615[12].
- primary ciliary dyskinesia 5's ICD-10-CM is recorded as Q34.8[13].
- primary ciliary dyskinesia 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- primary ciliary dyskinesia 5's Mondo ID is recorded as MONDO_0012088[15].
- primary ciliary dyskinesia 5's UniProt disease ID is recorded as DI-03560[16].