primary ciliary dyskinesia 20
Human disease
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primary ciliary dyskinesia 20
Summary
primary ciliary dyskinesia 20 is a rare disease[1].
Key Facts
- primary ciliary dyskinesia 20's instance of is recorded as rare disease[2].
- primary ciliary dyskinesia 20's instance of is recorded as class of disease[3].
- primary ciliary dyskinesia 20's subclass of is recorded as primary ciliary dyskinesia[4].
- primary ciliary dyskinesia 20's OMIM ID is recorded as 615067[5].
- primary ciliary dyskinesia 20's Disease Ontology ID is recorded as DOID:0110625[6].
- primary ciliary dyskinesia 20's health specialty is recorded as medical genetics[7].
- primary ciliary dyskinesia 20's genetic association is recorded as ODAD1[8].
- primary ciliary dyskinesia 20's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110625[9].
- primary ciliary dyskinesia 20's exact match is recorded as http://identifiers.org/doid/DOID:0110625[10].
- primary ciliary dyskinesia 20's UMLS CUI is recorded as C3540844[11].
- primary ciliary dyskinesia 20's ICD-10-CM is recorded as Q34.8[12].
- primary ciliary dyskinesia 20's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- primary ciliary dyskinesia 20's Mondo ID is recorded as MONDO_0014030[14].
- primary ciliary dyskinesia 20's UniProt disease ID is recorded as DI-03643[15].