primary ciliary dyskinesia 32
Human disease
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primary ciliary dyskinesia 32
Summary
primary ciliary dyskinesia 32 is a rare disease[1].
Key Facts
- primary ciliary dyskinesia 32's instance of is recorded as rare disease[2].
- primary ciliary dyskinesia 32's instance of is recorded as class of disease[3].
- primary ciliary dyskinesia 32's subclass of is recorded as primary ciliary dyskinesia[4].
- primary ciliary dyskinesia 32's OMIM ID is recorded as 616481[5].
- primary ciliary dyskinesia 32's Disease Ontology ID is recorded as DOID:0110603[6].
- primary ciliary dyskinesia 32's health specialty is recorded as medical genetics[7].
- primary ciliary dyskinesia 32's genetic association is recorded as RSPH3[8].
- primary ciliary dyskinesia 32's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110603[9].
- primary ciliary dyskinesia 32's exact match is recorded as http://identifiers.org/doid/DOID:0110603[10].
- primary ciliary dyskinesia 32's UMLS CUI is recorded as C4225311[11].
- primary ciliary dyskinesia 32's ICD-10-CM is recorded as Q34.8[12].
- primary ciliary dyskinesia 32's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- primary ciliary dyskinesia 32's Mondo ID is recorded as MONDO_0014657[14].
- primary ciliary dyskinesia 32's UniProt disease ID is recorded as DI-04489[15].