primary ciliary dyskinesia 2
Human disease
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primary ciliary dyskinesia 2
Summary
primary ciliary dyskinesia 2 is a rare disease[1].
Key Facts
- primary ciliary dyskinesia 2's instance of is recorded as rare disease[2].
- primary ciliary dyskinesia 2's instance of is recorded as class of disease[3].
- primary ciliary dyskinesia 2's subclass of is recorded as primary ciliary dyskinesia[4].
- primary ciliary dyskinesia 2's MeSH descriptor ID is recorded as C535277[5].
- primary ciliary dyskinesia 2's OMIM ID is recorded as 606763[6].
- primary ciliary dyskinesia 2's Disease Ontology ID is recorded as DOID:0110626[7].
- primary ciliary dyskinesia 2's health specialty is recorded as medical genetics[8].
- primary ciliary dyskinesia 2's genetic association is recorded as DNAAF3[9].
- primary ciliary dyskinesia 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110626[10].
- primary ciliary dyskinesia 2's exact match is recorded as http://identifiers.org/doid/DOID:0110626[11].
- primary ciliary dyskinesia 2's UMLS CUI is recorded as C1847554[12].
- primary ciliary dyskinesia 2's ICD-10-CM is recorded as Q34.8[13].
- primary ciliary dyskinesia 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- primary ciliary dyskinesia 2's Mondo ID is recorded as MONDO_0011718[15].
- primary ciliary dyskinesia 2's UniProt disease ID is recorded as DI-03362[16].