hypercholesterolemia, autosomal dominant, 3
human disease
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hypercholesterolemia, autosomal dominant, 3
Summary
hypercholesterolemia, autosomal dominant, 3 is a rare disease[1].
Key Facts
- hypercholesterolemia, autosomal dominant, 3's instance of is recorded as rare disease[2].
- hypercholesterolemia, autosomal dominant, 3's instance of is recorded as class of disease[3].
- hypercholesterolemia, autosomal dominant, 3's subclass of is recorded as disease[4].
- hypercholesterolemia, autosomal dominant, 3's MeSH descriptor ID is recorded as C566337[5].
- hypercholesterolemia, autosomal dominant, 3's OMIM ID is recorded as 603776[6].
- hypercholesterolemia, autosomal dominant, 3's Orphanet ID is recorded as 406[7].
- hypercholesterolemia, autosomal dominant, 3's genetic association is recorded as PCSK9[8].
- hypercholesterolemia, autosomal dominant, 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_406[9].
- hypercholesterolemia, autosomal dominant, 3's UMLS CUI is recorded as C3276239[10].
- hypercholesterolemia, autosomal dominant, 3's UMLS CUI is recorded as C1863551[11].
- hypercholesterolemia, autosomal dominant, 3's Mondo ID is recorded as MONDO_0011369[12].
- hypercholesterolemia, autosomal dominant, 3's ICD-11 ID is recorded as 357867015[13].
- hypercholesterolemia, autosomal dominant, 3's UniProt disease ID is recorded as DI-01578[14].