immunoglobulin A deficiency 2
human disease
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immunoglobulin A deficiency 2
Summary
immunoglobulin A deficiency 2 is a class of disease[1].
Key Facts
- immunoglobulin A deficiency 2's instance of is recorded as class of disease[2].
- immunoglobulin A deficiency 2's subclass of is recorded as immunoglobulin A deficiency[3].
- immunoglobulin A deficiency 2's MeSH descriptor ID is recorded as C536291[4].
- immunoglobulin A deficiency 2's OMIM ID is recorded as 609529[5].
- immunoglobulin A deficiency 2's Orphanet ID is recorded as 69127[6].
- immunoglobulin A deficiency 2's genetic association is recorded as TNFRSF13B[7].
- immunoglobulin A deficiency 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_69127[8].
- immunoglobulin A deficiency 2's UMLS CUI is recorded as C1836032[9].
- immunoglobulin A deficiency 2's GARD rare disease ID is recorded as 10198[10].
- immunoglobulin A deficiency 2's Mondo ID is recorded as MONDO_0012291[11].
- immunoglobulin A deficiency 2's UniProt disease ID is recorded as DI-01814[12].