primary ciliary dyskinesia 13
Human disease
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primary ciliary dyskinesia 13
Summary
primary ciliary dyskinesia 13 is a rare disease[1].
Key Facts
- primary ciliary dyskinesia 13's instance of is recorded as rare disease[2].
- primary ciliary dyskinesia 13's instance of is recorded as class of disease[3].
- primary ciliary dyskinesia 13's subclass of is recorded as primary ciliary dyskinesia[4].
- primary ciliary dyskinesia 13's MeSH descriptor ID is recorded as C567713[5].
- primary ciliary dyskinesia 13's OMIM ID is recorded as 613193[6].
- primary ciliary dyskinesia 13's Disease Ontology ID is recorded as DOID:0110618[7].
- primary ciliary dyskinesia 13's health specialty is recorded as medical genetics[8].
- primary ciliary dyskinesia 13's genetic association is recorded as DNAAF1[9].
- primary ciliary dyskinesia 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110618[10].
- primary ciliary dyskinesia 13's exact match is recorded as http://identifiers.org/doid/DOID:0110618[11].
- primary ciliary dyskinesia 13's UMLS CUI is recorded as C2750790[12].
- primary ciliary dyskinesia 13's ICD-10-CM is recorded as Q34.8[13].
- primary ciliary dyskinesia 13's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- primary ciliary dyskinesia 13's Mondo ID is recorded as MONDO_0013174[15].
- primary ciliary dyskinesia 13's UniProt disease ID is recorded as DI-02569[16].