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CTD Diseases (CD): CHOPS SYNDROME

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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)
+ + + + + 5:   Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] <5>(101|119) (108|51|28)
+ + + + 4:   Cardiovascular Diseases [MESH:D002318] <5>(37|36) (38|13|9)
+ + + + 4:   Signs and Symptoms [MESH:D012816] <38>(30|33) (33|13|1)
+ + + + 4:   Nutritional and Metabolic Diseases [MESH:D009750] <2>(51|55) (57|23|4)
+ + + + 4:   Pathological Conditions, Signs and Symptoms [MESH:D013568] <4>(81|94) (88|48|16)
+ + + + 4:   Congenital Abnormalities [MESH:D000013] <50>(37|46) (40|17|10)
+ + + 3:   Nutrition Disorders [MESH:D009748] <6>(2|2) (3|1|0)
+ + + 3:   Mental Disorders [MESH:D001523] <27>(22|26) (25|8|3)
+ + + 3:   Musculoskeletal Diseases [MESH:D009140] <13>(29|36) (36|21|18)
+ + + 3:   Diseases [MESH:C] <25>
+ + + 3:   Pathologic Processes [MESH:D010335] <65>(45|54) (50|27|12)
+ + + 3:   Heart Diseases [MESH:D006331] <31>(16|16) (19|5|4)
+ + + 3:   Body Weight [MESH:D001835] <5>(4|4) (5|2|0)
+ + + 3:   Cardiovascular Abnormalities [MESH:D018376] <6>(2|4) (3|1|2)
+ + 2:   Heart Defects, Congenital [MESH:D006330] <142>(2|4) (3|0|2)
+ + 2:   Overnutrition [MESH:D044343] <1>(2|2) (3|1|0)
+ + 2:   Respiratory Tract Diseases [MESH:D012140] <17>(20|24) (23|11|3)
+ + 2:   Overweight [MESH:D050177] <1>(3|3) (4|1|0)
+ + 2:   Disease Attributes [MESH:D020969] <20>(3|6) (3|6|4)
+ + 2:   Neurocognitive Disorders [MESH:D019965] <6>(5|2) (6|2|0)
+ + 2:   Bone Diseases [MESH:D001847] <34>(10|9) (12|6|4)
+ 1:   Heart Septal Defects [MESH:D006343] <13>(1|1) (1|0|0)
+ 1:   Facies [MESH:D019066] <151>(0|0) (0|0|0)
+ 1:   Obesity [MESH:D009765] <43>(0|0) (0|0|0)
+ 1:   Lung Diseases [MESH:D008171] <43>(16|19) (19|8|3)
+ 1:   Cognition Disorders [MESH:D003072] <8>(1|0) (1|0|0)
+ 1:   Bone Diseases, Developmental [MESH:D001848] <89>(2|4) (2|4|3)
0:   CHOPS SYNDROME [OMIM:616368](0|0) (0|0|0)