hyper-IgM syndrome type 2
human disease
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hyper-IgM syndrome type 2
Summary
hyper-IgM syndrome type 2 is a rare disease[1]. It draws 3 Wikipedia views per month (rare_disease category, ranking #235 of 627).[2]
Key Facts
- hyper-IgM syndrome type 2's instance of is recorded as rare disease[3].
- hyper-IgM syndrome type 2's instance of is recorded as class of disease[4].
- hyper-IgM syndrome type 2's subclass of is recorded as hyper IgM syndrome[5].
- hyper-IgM syndrome type 2's subclass of is recorded as hyperimmunoglobulin syndrome[6].
- hyper-IgM syndrome type 2's subclass of is recorded as genetic disease[7].
- hyper-IgM syndrome type 2's subclass of is recorded as autosomal recessive disease[8].
- hyper-IgM syndrome type 2's OMIM ID is recorded as 605258[9].
- hyper-IgM syndrome type 2's KEGG ID is recorded as H00086[10].
- hyper-IgM syndrome type 2's Disease Ontology ID is recorded as DOID:0060758[11].
- hyper-IgM syndrome type 2's Orphanet ID is recorded as 183666[12].
- hyper-IgM syndrome type 2's Orphanet ID is recorded as 101089[13].
- hyper-IgM syndrome type 2's NCI Thesaurus ID is recorded as C129074[14].
- hyper-IgM syndrome type 2's genetic association is recorded as AICDA[15].
- hyper-IgM syndrome type 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060758[16].
- hyper-IgM syndrome type 2's exact match is recorded as http://identifiers.org/doid/DOID:0060758[17].
- hyper-IgM syndrome type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_101089[18].
- hyper-IgM syndrome type 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_183666[19].
- hyper-IgM syndrome type 2's UMLS CUI is recorded as C1720956[20].
- hyper-IgM syndrome type 2's ICD-10-CM is recorded as D80.5[21].
- hyper-IgM syndrome type 2's GARD rare disease ID is recorded as 10578[22].
- hyper-IgM syndrome type 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[23].
- hyper-IgM syndrome type 2's Mondo ID is recorded as MONDO_0011528[24].
- hyper-IgM syndrome type 2's Microsoft Academic ID is recorded as 2779925706[25].
- hyper-IgM syndrome type 2's UniProt disease ID is recorded as DI-01241[26].
Why It Matters
hyper-IgM syndrome type 2 draws 3 Wikipedia views per month (rare_disease category, ranking #235 of 627).[2]