C2936380 |
Neointima
|
disease |
Pathological Conditions, Signs and Symptoms
|
Acquired Abnormality
|
|
|
33 |
C0600033 |
Acquired Kyphoscoliosis
|
disease |
Musculoskeletal Diseases
|
Acquired Abnormality
|
|
|
4 |
C0156181 |
Peritoneal adhesion
|
disease |
Digestive System Diseases; Skin and Connective Tissue Diseases
|
Acquired Abnormality
|
|
|
2 |
C0740391 |
Middle Cerebral Artery Occlusion
|
disease |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
|
Acquired Abnormality
|
|
|
1 |
C3698507 |
Post-traumatic Porencephaly
|
phenotype |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
|
Acquired Abnormality
|
disease of anatomical entity
|
|
1 |
C0029866 |
Other ureteric obstruction
|
phenotype |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
|
Anatomical Abnormality
|
disease of anatomical entity
|
|
52 |
C0003855 |
Arteriovenous fistula
|
phenotype |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
Anatomical Abnormality
|
|
Abnormality of the cardiovascular system
|
12 |
C3495676 |
Anorectal Malformations
|
group |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
|
Anatomical Abnormality
|
disease of anatomical entity
|
Abnormality of the digestive system
|
6 |
C0024636 |
Malocclusion
|
disease |
Stomatognathic Diseases
|
Anatomical Abnormality
|
|
Abnormality of head or neck
|
4 |
C0575158 |
Kyphoscoliosis deformity of spine
|
disease |
Musculoskeletal Diseases
|
Anatomical Abnormality
|
disease of anatomical entity
|
Abnormality of the skeletal system
|
4 |
C0009917 |
Contracture
|
disease |
Musculoskeletal Diseases
|
Anatomical Abnormality
|
|
Abnormality of the skeletal system; Abnormality of connective tissue; Abnormality of the musculature
|
2 |
C0019326 |
Ventral Hernia
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Anatomical Abnormality
|
|
Abnormality of the digestive system; Abnormality of connective tissue
|
2 |
C0040588 |
Tracheoesophageal Fistula
|
disease |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Respiratory Tract Diseases
|
Anatomical Abnormality
|
|
Abnormality of the digestive system; Abnormality of the respiratory system
|
2 |
C0006262 |
Bronchial Fistula
|
disease |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
|
Anatomical Abnormality
|
|
|
1 |
C0009376 |
Colonic Polyps
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Anatomical Abnormality
|
|
|
1 |
C0021833 |
Intestinal Fistula
|
phenotype |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases
|
Anatomical Abnormality
|
|
Abnormality of the digestive system
|
1 |
C1849930 |
Persistent Mullerian duct syndrome
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
|
Anatomical Abnormality
|
disease of anatomical entity
|
|
1 |
C2919945 |
Cavernous Hemangioma of Brain
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
|
Anatomical Abnormality
|
disease of anatomical entity
|
|
1 |
C0043020 |
Wallerian Degeneration
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Cell or Molecular Dysfunction
|
|
|
17 |
C0027746 |
Nerve Degeneration
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Cell or Molecular Dysfunction
|
|
Abnormality of the nervous system
|
10 |
C0025568 |
Metaplasia
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Cell or Molecular Dysfunction
|
|
|
2 |
C0035354 |
Retrograde Degeneration
|
phenotype |
Pathological Conditions, Signs and Symptoms
|
Cell or Molecular Dysfunction
|
|
|
1 |
C0009691 |
Congenital cataract
|
disease |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Eye Diseases; Nervous System Diseases
|
Congenital Abnormality
|
genetic disease; disease of anatomical entity
|
Abnormality of the eye
|
17 |
C0010417 |
Cryptorchidism
|
disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases
|
Congenital Abnormality
|
physical disorder
|
Abnormality of the genitourinary system
|
14 |
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
|
13 |