Source: BEFREE

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes Num. SNPs
C1290073 Acute mucositis disease Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Stomatognathic Diseases Disease or Syndrome 1 1
C1832273 Ribbing disease disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases Disease or Syndrome 1 1
C0015263 Bronchospasm, Exercise-Induced disease Respiratory Tract Diseases; Immune System Diseases Disease or Syndrome 1 0
C0030590 Paroxysmal supraventricular tachycardia disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome Abnormality of the cardiovascular system 1 0
C0037942 Spinal Osteophytosis disease Musculoskeletal Diseases Disease or Syndrome 1 0
C0156318 Fibrosclerosis of breast disease Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity; disease of cellular proliferation 1 0
C0221745 Depression suicidal disease Mental Disorders Mental or Behavioral Dysfunction 1 0
C0585473 Chondromyxoid fibroma of bone disease Neoplastic Process 1 0
C1266165 High grade surface osteosarcoma disease Neoplastic Process 1 0
C1335169 Ovarian Adenosarcoma disease Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation 1 0
C1859047 CYSTIC FIBROSIS MODIFIER 1 disease Disease or Syndrome 1 0
C2242653 Thyroid fibrosis disease Disease or Syndrome 1 0
C3544328 Prostatic fibrosis disease Disease or Syndrome 1 0
C4024975 Posterior leukoencephalopathy disease Nervous System Diseases Disease or Syndrome Abnormality of the nervous system 1 0
C0041105 Trismus disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome Abnormality of head or neck; Abnormality of the skeletal system 2 0
C0242520 Chronic thyroiditis disease Endocrine System Diseases Disease or Syndrome disease of anatomical entity 2 0
C0392170 Fibrotic lymphadenopathy disease Hemic and Lymphatic Diseases Disease or Syndrome 2 0
C0854260 Congenital urinary tract obstruction disease Congenital Abnormality 2 0
C1969236 Mitten deformity phenotype Congenital Abnormality Abnormality of limbs 2 0
C2586331 Surrogate mother (family issue) disease Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 2 0
C3872845 Idiopathic eosinophilic pneumonia disease Infections; Respiratory Tract Diseases; Hemic and Lymphatic Diseases Disease or Syndrome 2 0
C4042788 Left-Sided Breast Neoplasms disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process 2 0
C0162281 Corneal deposit disease Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases Disease or Syndrome disease of anatomical entity 3 3
C0015645 Fasciitis disease Musculoskeletal Diseases Disease or Syndrome disease of anatomical entity Abnormality of the immune system; Abnormality of connective tissue 3 0
C0263664 Generalized morphea disease Skin and Connective Tissue Diseases Disease or Syndrome 3 0