hypercholesterolemia, autosomal dominant, type b
human disease
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hypercholesterolemia, autosomal dominant, type b
Summary
hypercholesterolemia, autosomal dominant, type b is a rare disease[1].
Key Facts
- hypercholesterolemia, autosomal dominant, type b's instance of is recorded as rare disease[2].
- hypercholesterolemia, autosomal dominant, type b's instance of is recorded as class of disease[3].
- hypercholesterolemia, autosomal dominant, type b's subclass of is recorded as familial hypercholesterolemia[4].
- hypercholesterolemia, autosomal dominant, type b's OMIM ID is recorded as 144010[5].
- hypercholesterolemia, autosomal dominant, type b's Orphanet ID is recorded as 406[6].
- hypercholesterolemia, autosomal dominant, type b's genetic association is recorded as APOB[7].
- hypercholesterolemia, autosomal dominant, type b's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_406[8].
- hypercholesterolemia, autosomal dominant, type b's UMLS CUI is recorded as C1704417[9].
- hypercholesterolemia, autosomal dominant, type b's UMLS CUI is recorded as C2931106[10].
- hypercholesterolemia, autosomal dominant, type b's GARD rare disease ID is recorded as 8588[11].
- hypercholesterolemia, autosomal dominant, type b's Mondo ID is recorded as MONDO_0007751[12].
- hypercholesterolemia, autosomal dominant, type b's ICD-11 ID is recorded as 2106114192[13].