MonoMAC
disease
Press Enter · cited answer in seconds
0 sources
MonoMAC
Summary
MonoMAC is a rare disease[1]. MonoMAC draws 25 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 is a type of primary immunodeficiency disease[5].
- MonoMAC is a type of quantitative and/or qualitative congenital phagocyte defect[6].
- MonoMAC is a type of GATA2 deficiency[7].
- MonoMAC is a type of autosomal dominant disease[8].
- MonoMAC's symptoms and signs is recorded as monocytopenia[9].
- MonoMAC's health specialty is recorded as medical genetics[10].
- MonoMAC's genetic association is recorded as GATA2[11].
- MonoMAC's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_228423[12].
- MonoMAC's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111947[13].
- MonoMAC's exact match is recorded as http://identifiers.org/doid/DOID:0111947[14].
Why It Matters
MonoMAC draws 25 Wikipedia views per month (rare_disease category, ranking #234 of 627).[2]