hyper-IgM syndrome type 5
human disease
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hyper-IgM syndrome type 5
Summary
hyper-IgM syndrome type 5 is a rare disease[1]. It is known by 11 alternative names across languages and contexts.[2]
Key Facts
- hyper-IgM syndrome type 5's instance of is recorded as rare disease[3].
- hyper-IgM syndrome type 5's instance of is recorded as class of disease[4].
- hyper-IgM syndrome type 5 is a type of hyper IgM syndrome[5].
- hyper-IgM syndrome type 5 is a type of hyperimmunoglobulin syndrome[6].
- hyper-IgM syndrome type 5 is a type of genetic disease[7].
- hyper-IgM syndrome type 5 is a type of autosomal recessive disease[8].
- hyper-IgM syndrome type 5's genetic association is recorded as UNG[9].
- hyper-IgM syndrome type 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060759[10].
- hyper-IgM syndrome type 5's exact match is recorded as http://identifiers.org/doid/DOID:0060759[11].
- hyper-IgM syndrome type 5's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101092[12].
- hyper-IgM syndrome type 5's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_183666[13].
- hyper-IgM syndrome type 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
hyper-IgM syndrome type 5 is known by 11 alternative names across languages and contexts.[2]