Source: MGD

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0007193 Cardiomyopathy, Dilated group Cardiovascular Diseases Disease or Syndrome disease of anatomical entity Abnormality of the cardiovascular system 44
C0004352 Autistic Disorder group Mental Disorders Mental or Behavioral Dysfunction disease of mental health Abnormality of the nervous system 42
C0154860 Hereditary retinal dystrophy group Disease or Syndrome disease of anatomical entity; genetic disease 39
C0029838 Other specified types of schizophrenia, unspecified disease Mental or Behavioral Dysfunction disease of mental health 37
C0220702 SCHIZOPHRENIA 1 (disorder) disease Mental or Behavioral Dysfunction disease of mental health 37
C0024141 Lupus Erythematosus, Systemic disease Immune System Diseases; Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity Abnormality of the immune system 32
C0452138 Sensorineural hearing loss, bilateral disease Disease or Syndrome disease of anatomical entity Abnormality of the ear 32
C0028754 Obesity disease Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms Disease or Syndrome disease of metabolism Growth abnormality 30
C0011860 Diabetes Mellitus, Non-Insulin-Dependent disease Endocrine System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome disease of metabolism Abnormality of metabolism/homeostasis; Abnormality of the endocrine system 29
C1415817 HETEROTAXY, VISCERAL, 2, AUTOSOMAL disease Disease or Syndrome physical disorder 29
C1844020 HETEROTAXY, VISCERAL, 1, X-LINKED disease Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome physical disorder 29
C1853444 Heterotaxy, Visceral, 3, Autosomal disease Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases Disease or Syndrome physical disorder 29
C3151057 HETEROTAXY, VISCERAL, 4, AUTOSOMAL disease Disease or Syndrome physical disorder 29
C3151867 CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED disease Disease or Syndrome physical disorder 29
C3553676 HETEROTAXY, VISCERAL, 6, AUTOSOMAL disease Disease or Syndrome physical disorder 29
C0011854 Diabetes Mellitus, Insulin-Dependent disease Endocrine System Diseases; Immune System Diseases; Nutritional and Metabolic Diseases Disease or Syndrome disease of metabolism Abnormality of metabolism/homeostasis; Abnormality of the endocrine system 22
C0029882 Otitis Media disease Otorhinolaryngologic Diseases Disease or Syndrome disease of anatomical entity Abnormality of the ear; Abnormality of the immune system 19
C0020255 Hydrocephalus disease Nervous System Diseases Disease or Syndrome disease of anatomical entity Abnormality of the nervous system 18
C0027888 Hereditary Motor and Sensory Neuropathies group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome disease of anatomical entity 18
C0006142 Malignant neoplasm of breast disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process disease of anatomical entity; disease of cellular proliferation 17
C0007959 Charcot-Marie-Tooth Disease disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome disease of anatomical entity 17
C0009691 Congenital cataract disease Congenital Abnormality disease of anatomical entity Abnormality of the eye 17
C0011195 Dejerine-Sottas Disease (disorder) disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Disease or Syndrome disease of anatomical entity 17
C0086981 Sicca Syndrome disease Eye Diseases; Immune System Diseases; Musculoskeletal Diseases; Skin and Connective Tissue Diseases; Stomatognathic Diseases Disease or Syndrome disease of anatomical entity 17
C0153555 Malignant neoplasm of other specified sites of female breast disease Neoplastic Process disease of anatomical entity; disease of cellular proliferation 17