homozygous familial hypercholesterolemia
human disease
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Summary
homozygous familial hypercholesterolemia is a designated intractable/rare disease[1].
Key Facts
- homozygous familial hypercholesterolemia's instance of is recorded as designated intractable/rare disease[2].
- homozygous familial hypercholesterolemia's instance of is recorded as class of disease[3].
- homozygous familial hypercholesterolemia's subclass of is recorded as familial hypercholesterolemia[4].
- homozygous familial hypercholesterolemia's MeSH descriptor ID is recorded as D000090542[5].
- homozygous familial hypercholesterolemia's MeSH tree code is recorded as C16.320.565.398.481.500[6].
- homozygous familial hypercholesterolemia's MeSH tree code is recorded as C18.452.584.500.500.644.475.500[7].
- homozygous familial hypercholesterolemia's MeSH tree code is recorded as C18.452.584.563.481.500[8].
- homozygous familial hypercholesterolemia's MeSH tree code is recorded as C18.452.648.398.481.500[9].
- homozygous familial hypercholesterolemia's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/65[10].
- homozygous familial hypercholesterolemia's Orphanet ID is recorded as 391665[11].
- homozygous familial hypercholesterolemia's genetic association is recorded as LDLRAP1[12].
- homozygous familial hypercholesterolemia's Google Knowledge Graph ID is recorded as /g/1ym_k_c84[13].
- homozygous familial hypercholesterolemia's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_391665[14].
- homozygous familial hypercholesterolemia's UMLS CUI is recorded as C0342881[15].
- homozygous familial hypercholesterolemia's ICD-10-CM is recorded as E78.0[16].
- homozygous familial hypercholesterolemia's Mondo ID is recorded as MONDO_0018328[17].
- homozygous familial hypercholesterolemia's ICD-11 ID is recorded as 1525871199[18].