MonoMAC
disease
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MonoMAC
Summary
MonoMAC is a rare disease[1]. MonoMAC draws 5 Wikipedia views per month (rare_disease category, ranking #234 of 627).[2]
Key Facts
- MonoMAC's instance of is recorded as rare disease[3].
- MonoMAC's instance of is recorded as class of disease[4].
- MonoMAC's subclass of is recorded as primary immunodeficiency disease[5].
- MonoMAC's subclass of is recorded as quantitative and/or qualitative congenital phagocyte defect[6].
- MonoMAC's subclass of is recorded as GATA2 deficiency[7].
- MonoMAC's subclass of is recorded as autosomal dominant disease[8].
- MonoMAC's OMIM ID is recorded as 614172[9].
- MonoMAC's Disease Ontology ID is recorded as DOID:0111947[10].
- MonoMAC's symptoms and signs is recorded as monocytopenia[11].
- MonoMAC's Orphanet ID is recorded as 228423[12].
- MonoMAC's health specialty is recorded as medical genetics[13].
- MonoMAC's genetic association is recorded as GATA2[14].
- MonoMAC's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_228423[15].
- MonoMAC's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111947[16].
- MonoMAC's exact match is recorded as http://identifiers.org/doid/DOID:0111947[17].
- MonoMAC's UMLS CUI is recorded as C3280030[18].
- MonoMAC's ICD-10-CM is recorded as D72.8[19].
- MonoMAC's GARD rare disease ID is recorded as 10934[20].
- MonoMAC's Mondo ID is recorded as MONDO_0013607[21].
- MonoMAC's Microsoft Academic ID is recorded as 2780711755[22].
- MonoMAC's UniProt disease ID is recorded as DI-03212[23].
Why It Matters
MonoMAC draws 5 Wikipedia views per month (rare_disease category, ranking #234 of 627).[2]