Source: CTD_mouse

CUI Disease Type Disease Class Semantic type DO Class HPO Term Num. genes
C0497552 Congenital neurologic anomalies group Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality Abnormality of the nervous system 1
C0265541 Cranioschisis disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases Congenital Abnormality 1
C0746857 Focal Neurologic Deficits phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 1
C0521654 Neurologic Deficits group Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 1
C0751377 Neurologic Dysfunction phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 1
C0027854 Neurologic Manifestations phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 1
C0751378 Neurologic Signs phenotype Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 1
C0235031 Neurologic Symptoms group Pathological Conditions, Signs and Symptoms; Nervous System Diseases Sign or Symptom 1
C0422837 Neurological observations group Pathological Conditions, Signs and Symptoms; Nervous System Diseases Finding 1