C0022548 |
Keloid
|
disease |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
|
Acquired Abnormality
|
|
Abnormality of the integument; Abnormality of connective tissue
|
1 |
4 |
C0410702 |
Adolescent idiopathic scoliosis
|
disease |
Musculoskeletal Diseases
|
Anatomical Abnormality
|
|
|
3 |
7 |
C0032176 |
Platelet aggregation
|
phenotype |
|
Cell Function
|
|
|
7 |
11 |
C3547188 |
response to fenofibrate
|
phenotype |
|
Cell Function
|
|
|
4 |
5 |
C3547187 |
response to metformin
|
phenotype |
|
Cell Function
|
|
|
3 |
14 |
C3546688 |
response to temozolomide
|
phenotype |
|
Cell Function
|
|
|
1 |
1 |
C1305855 |
Body mass index
|
phenotype |
|
Clinical Attribute
|
|
|
24 |
29 |
C0429028 |
QT interval feature (observable entity)
|
phenotype |
|
Clinical Attribute
|
|
|
23 |
99 |
C0005938 |
Bone Density
|
phenotype |
|
Clinical Attribute
|
|
|
22 |
350 |
C0018810 |
heart rate
|
phenotype |
|
Clinical Attribute
|
|
|
17 |
32 |
C0455829 |
Waist Circumference
|
phenotype |
|
Clinical Attribute
|
|
|
8 |
81 |
C1328319 |
Ankle brachial pressure index (observable entity)
|
phenotype |
|
Clinical Attribute
|
|
|
5 |
33 |
C0424678 |
Lean body mass
|
phenotype |
|
Clinical Attribute
|
|
|
3 |
5 |
C0008924 |
Cleft upper lip
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
|
Congenital Abnormality
|
disease of anatomical entity; syndrome; physical disorder
|
Abnormality of head or neck
|
21 |
172 |
C0039685 |
Tetralogy of Fallot
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
disease of anatomical entity
|
Abnormality of the cardiovascular system
|
9 |
14 |
C0700639 |
Pyloric Stenosis, Hypertrophic
|
disease |
Digestive System Diseases
|
Congenital Abnormality
|
disease of anatomical entity
|
|
9 |
298 |
C0005411 |
Biliary Atresia
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
|
Congenital Abnormality
|
disease of anatomical entity
|
Abnormality of the digestive system
|
8 |
12 |
C1853238 |
Conotruncal defect
|
disease |
|
Congenital Abnormality
|
|
Abnormality of the cardiovascular system
|
2 |
7 |
C0009081 |
Congenital clubfoot
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
disease of anatomical entity
|
Abnormality of limbs
|
1 |
1 |
C0018798 |
Congenital Heart Defects
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
disease of anatomical entity
|
Abnormality of the cardiovascular system
|
1 |
2 |
C0149630 |
Bicuspid aortic valve
|
disease |
Cardiovascular Diseases
|
Congenital Abnormality
|
disease of anatomical entity
|
Abnormality of the cardiovascular system
|
1 |
1 |
C0152021 |
Congenital heart disease
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
disease of anatomical entity
|
Abnormality of the cardiovascular system
|
1 |
3 |
C0158611 |
Other congenital anomalies of heart
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
|
|
1 |
2 |
C0432123 |
Sagittal craniosynostosis
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
|
Congenital Abnormality
|
|
Abnormality of head or neck; Abnormality of the skeletal system
|
1 |
2 |
C0478009 |
Congenital malformation of cardiac chambers and connections, unspecified
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Congenital Abnormality
|
|
|
1 |
2 |