Source: RGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
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
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
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 8
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
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 12
C0848558 Hypospadias disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Congenital Abnormality physical disorder Abnormality of the genitourinary system 6
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 4
C0345392 Congenital kyphoscoliosis disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality Abnormality of the skeletal system 4
C0013336 Dwarfism disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases Congenital Abnormality genetic disease Growth abnormality 3
C0037917 Spina Bifida Cystica disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality disease of anatomical entity; physical disorder 3
C0026010 Microphthalmos disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases Congenital Abnormality disease of anatomical entity Abnormality of the eye 2