Source: CURATED

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C0086543 Cataract disease Eye Diseases Acquired Abnormality genetic disease; disease of anatomical entity Abnormality of the eye 37 13
C0022548 Keloid disease Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases Acquired Abnormality Abnormality of the integument; Abnormality of connective tissue 35 4
C0740391 Middle Cerebral Artery Occlusion disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 34 0
C2936380 Neointima disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 6 0
C0015697 Arterial Fatty Streak phenotype Pathological Conditions, Signs and Symptoms Acquired Abnormality 5 0
C0086501 Keratoma disease Skin and Connective Tissue Diseases Acquired Abnormality 5 0
C0751633 Carotid Artery Plaque disease Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 5 0
C0751634 Carotid Ulcer phenotype Nervous System Diseases; Cardiovascular Diseases Acquired Abnormality 5 0
C2936351 Fibroatheroma disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 5 0
C0751316 Acquired Meningomyelocele phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Acquired Abnormality disease of anatomical entity; physical disorder 4 0
C0333463 Senile Plaques disease Pathological Conditions, Signs and Symptoms Acquired Abnormality Abnormality of the nervous system 2 0
C2936349 Plaque, Amyloid disease Pathological Conditions, Signs and Symptoms Acquired Abnormality 2 0
C3698507 Post-traumatic Porencephaly phenotype Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases Acquired Abnormality disease of anatomical entity 2 0
C0014849 Esophageal and Gastric Varices disease Digestive System Diseases Acquired Abnormality 1 0
C0016427 Follicular cyst disease Neoplasms Acquired Abnormality 1 0
C0033793 Pseudocoloboma phenotype Acquired Abnormality 1 0
C0158489 Acquired clubfoot disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases; Musculoskeletal Diseases Acquired Abnormality 1 0
C0235259 Subcapsular cataract disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Acquired Abnormality Abnormality of the eye 1 1
C0267211 Gastric Antral Vascular Ectasia disease Digestive System Diseases; Cardiovascular Diseases Acquired Abnormality disease of anatomical entity 1 0
C2880562 Age-related cortical cataract disease Acquired Abnormality Abnormality of the eye 1 0
C0041960 Ureterocele disease Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases Acquired Abnormality disease of anatomical entity Abnormality of the genitourinary system 0 1
C0152459 Linear atrophy disease Pathological Conditions, Signs and Symptoms Acquired Abnormality Abnormality of the integument 0 6
C0158465 Acquired cubitus valgus disease Acquired Abnormality Abnormality of limbs; Abnormality of the skeletal system 0 1
C0264162 Camptocormia disease Musculoskeletal Diseases; Nervous System Diseases Acquired Abnormality Abnormality of the skeletal system 0 2
C0281899 Prolapsed lumbar disc disease Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases Acquired Abnormality 0 1