pancytopenia due to IKZF1 mutations
human disease
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pancytopenia due to IKZF1 mutations
Summary
pancytopenia due to IKZF1 mutations is a rare disease[1].
Key Facts
- pancytopenia due to IKZF1 mutations's instance of is recorded as rare disease[2].
- pancytopenia due to IKZF1 mutations's instance of is recorded as class of disease[3].
- pancytopenia due to IKZF1 mutations's subclass of is recorded as syndrome with combined immunodeficiency[4].
- pancytopenia due to IKZF1 mutations's subclass of is recorded as common variable immunodeficiency[5].
- pancytopenia due to IKZF1 mutations's OMIM ID is recorded as 616873[6].
- pancytopenia due to IKZF1 mutations's Orphanet ID is recorded as 317473[7].
- pancytopenia due to IKZF1 mutations's genetic association is recorded as IKZF1[8].
- pancytopenia due to IKZF1 mutations's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_317473[9].
- pancytopenia due to IKZF1 mutations's UMLS CUI is recorded as C4225173[10].
- pancytopenia due to IKZF1 mutations's UMLS CUI is recorded as C5190826[11].
- pancytopenia due to IKZF1 mutations's ICD-10-CM is recorded as D81.8[12].
- pancytopenia due to IKZF1 mutations's Mondo ID is recorded as MONDO_0014810[13].
- pancytopenia due to IKZF1 mutations's UniProt disease ID is recorded as DI-04688[14].