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CTD Diseases (CD): Hypercholesterolemia

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Root: CD Hierarchy (CTD diseases from Comparative Toxicogenomics Database)

Shortest distance to current term
(+ for parents, - for children)
CD term [CD ID] <#Children> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + + + 6:   Diseases [MESH:C] <25>
+ + + + + 5:   Nutritional and Metabolic Diseases [MESH:D009750] <2>(51|55) (57|23|4)
+ + + + 4:   Metabolic Diseases [MESH:D008659] <23>(49|55) (54|22|4)
+ + + 3:   Lipid Metabolism Disorders [MESH:D052439] <7>(4|3) (4|1|0)
+ + 2:   Dyslipidemias [MESH:D050171] <14>(1|2) (1|0|0)
+ 1:   Hyperlipidemias [MESH:D006949] <5>(1|2) (1|0|0)
0:   Hypercholesterolemia [MESH:D006937] <5>(0|1) (0|0|0)
- 1:   CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 1 [OMIM:604595](0|0) (0|0|0)
- 1:   HYPERCHOLESTEROLEMIA, FAMILIAL, 1 [OMIM:143890](0|0) (0|0|0)
- 1:   Hypercholesterolemia, Autosomal Recessive [MESH:C566331](0|0) (0|0|0)
- 1:   Hypomagnesemia, Hypertension, and Hypercholesterolemia, Mitochondrial [MESH:C564024](0|0) (0|0|0)
- 1:   Sitosterolemia [MESH:C537345](0|0) (0|0|0)