Source: CTD_mouse

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0149958 Complex partial seizures disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome Abnormality of the nervous system 1
C0393734 Complex Partial Status Epilepticus disease Pathological Conditions, Signs and Symptoms; Nervous System Diseases Disease or Syndrome 1
C0282313 Condition, Preneoplastic disease Neoplasms Neoplastic Process 1
C0497552 Congenital neurologic anomalies group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality Abnormality of the nervous system 1
C4048158 Convulsions phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 1
C0751494 Convulsive Seizures phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 1
C0376634 Craniofacial Abnormalities group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases Congenital Abnormality 1
C0265541 Cranioschisis disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 1
C1136033 Cutaneous Mastocytosis disease Neoplasms; Skin and Connective Tissue Diseases Neoplastic Process disease of anatomical entity Abnormality of the integument; Abnormality of the immune system; Neoplasm; Abnormality of blood and blood-forming tissues 1
C0270715 Degenerative Diseases, Central Nervous System group Nervous System Diseases Disease or Syndrome disease of anatomical entity 1
C0751733 Degenerative Diseases, Spinal Cord group Nervous System Diseases Disease or Syndrome 1
C0011303 Demyelinating Diseases group Nervous System Diseases Disease or Syndrome disease of anatomical entity 1
C0011304 Demyelination phenotype Nervous System Diseases Pathologic Function 1
C0037274 Dermatologic disorders group Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity Abnormality of the integument 1
C0011854 Diabetes Mellitus, Insulin-Dependent disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome genetic disease; disease of metabolism Abnormality of metabolism/homeostasis; Abnormality of the endocrine system 1
C3837958 Diabetes Mellitus, Ketosis-Prone disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome genetic disease; disease of metabolism 1
C4554117 Diabetes Mellitus, Sudden-Onset disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 1
C0205734 Diabetes, Autoimmune disease Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases Disease or Syndrome 1
C0019284 Diaphragmatic Hernia phenotype Pathological Conditions, Signs and Symptoms Disease or Syndrome disease of anatomical entity 1
C0280785 Diffuse Astrocytoma disease Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation 1
C0015397 Disorder of eye group Eye Diseases Disease or Syndrome disease of anatomical entity Abnormality of the eye 1
C0013182 Drug Allergy group Immune System Diseases; Chemically-Induced Disorders Pathologic Function 1
C1176475 Ductal Carcinoma disease Neoplasms Neoplastic Process disease of anatomical entity; disease of cellular proliferation 1
C0013595 Eczema disease Skin and Connective Tissue Diseases Disease or Syndrome disease of anatomical entity Abnormality of the integument; Abnormality of the immune system 1
C0751847 Embolic Infarction, Middle Cerebral Artery phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases Disease or Syndrome 1