All terms in DOID

Label Id Description
chronic ulcer of skin DOID_8549
obsolete lymphosarcoma and reticulosarcoma DOID_8716
abnormal hemiwalking SYMP_0000670
cleft palate-lateral synechia syndrome DOID_0080313 [A physical disorder that is characterized by fusion of maxilla and mandible.]
cone-rod dystrophy 14 DOID_0080314 [A cone-rod dystrophy that is characterized by deterioration of the cone in childhood or early adult life and progressive deterioration of the rod photoreceptor cells in later life that has_material_basis_in mutation in the GUCA1A gene on chromosome 6p21.1.]
megalencephalic leukoencephalopathy with subcortical cysts DOID_0080315 [A leukodystorphy characterized by infantile-onset macrocephaly, often with mild neurologic signs at presentation (such as mild motor delay), which worse with time, leading to poor ambulation, falls, ataxia, spasticity, increasing seizures and cognitive decline.]
megalencephalic leukoencephalopathy with subcortical cysts 1 DOID_0080316 [A megalencephalic leukoencephalopathy with subcortical cysts characterized by early-onset macrocephaly and delayed-onset neurologic deterioration, including cerebellar ataxia, spasticity, epilepsy, and mild cognitive decline, that has_material_basis_in homozygous or compound heterozygous mutation in the MLC1 gene on chromosome 22q13.]
circling movement SYMP_0000688 [An abnormal involuntary movement that is characterized by an inability to walk in a straight line.]
Billuart-type X-linked syndromic intellectual developmental disorder DOID_0080311 [A syndromic X-linked intellectual disability characterized by moderately to severely impaired intellectual development, cerebellar hypoplasia, and seizures that has_material_basis_in mutation in the oligophrenin-1 gene on chromosome Xq12.]
cramp SYMP_0000689
neurodevelopmental disorder with midbrain and hindbrain malformations DOID_0080312 [A syndromic intellectual disability characterized by mild microcephaly, midbrain-hindbrain malformations, decreased reflexes, impaired fine motor movements, and variable dysmorphic features that has_material_basis_in homozygous mutation in the ARHGEF2 gene on chromosome 1q22.]
Poeae NCBITaxon_147387
megalencephalic leukoencephalopathy with subcortical cysts 2B DOID_0080317 [A megalencephalic leukoencephalopathy with subcortical cysts characterized by infantile-onset macrocephaly and mildly delayed motor development associated with white matter abnormalities that improve with age, and sometimes mental retardation that has_material_basis_in heterozygous mutation in the HEPACAM gene on chromosome 11q24.]
megalencephalic leukoencephalopathy with subcortical cysts 2A DOID_0080318 [A megalencephalic leukoencephalopathy with subcortical cysts characterized by infantile-onset macrocephaly and later onset of motor deterioration, with ataxia and spasticity, seizures, cognitive decline of variable severity, white matter abnormalities, including swelling of the cerebral white matter and subcortical cysts that has_material_basis_in homozygous or compound heterozygous mutation in the HEPACAM gene on chromosome 11q24.]
X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia DOID_0080319 [A T cell deficiency that is characterized by CD4 lymphopenia, severe chronic viral infections, and defective T-lymphocyte activation in males and has_material_basis_in X-linked inheritance of mutations in the gene encoding magnesium transporter-1 (MAGT1).]
vascular dementia DOID_8725 [A dementia that involves impairments in cognitive function caused by problems in blood vessels that feed the brain.]
dementia DOID_1307 [A cognitive disorder resulting from a loss of brain function affecting memory, thinking, language, judgement and behavior.]
chronic cough SYMP_0000686 [A cough that is characterized by an explosive expulsion of air from the lungs acting as a protective mechanism to clear the air passages or as a symptom of pulmonary disturbance marked by long duration, by frequent recurrence over a long time, and often by slowly progressing seriousness.]
bifrontal headache SYMP_0000684
brain cyst SYMP_0000685