complement component 9 deficiency
Human disease
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complement component 9 deficiency
Summary
complement component 9 deficiency is a rare disease[1].
Key Facts
- complement component 9 deficiency's instance of is recorded as rare disease[2].
- complement component 9 deficiency's instance of is recorded as class of disease[3].
- complement component 9 deficiency's subclass of is recorded as complement deficiency[4].
- complement component 9 deficiency's MeSH descriptor ID is recorded as C565165[5].
- complement component 9 deficiency's OMIM ID is recorded as 613825[6].
- complement component 9 deficiency's Disease Ontology ID is recorded as DOID:0060303[7].
- complement component 9 deficiency's Orphanet ID is recorded as 169150[8].
- complement component 9 deficiency's genetic association is recorded as C9[9].
- complement component 9 deficiency's genetic association is recorded as C6[10].
- complement component 9 deficiency's genetic association is recorded as C7[11].
- complement component 9 deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060303[12].
- complement component 9 deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0060303[13].
- complement component 9 deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_169150[14].
- complement component 9 deficiency's UMLS CUI is recorded as C3151189[15].
- complement component 9 deficiency's UMLS CUI is recorded as C0398765[16].
- complement component 9 deficiency's ICD-10-CM is recorded as D84.1[17].
- complement component 9 deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
- complement component 9 deficiency's Mondo ID is recorded as MONDO_0013445[19].
- complement component 9 deficiency's ICD-11 ID is recorded as 446269999[20].
- complement component 9 deficiency's UniProt disease ID is recorded as DI-01383[21].