All terms in DOID

Label Id Description
obsolete recurrent childhood central nervous system tumor DOID_6384
melioidosis DOID_5052 [A primary bacterial infectious disease that results_in infection, has_material_basis_in Burkholderia pseudomallei, which is transmitted_by contact with the contaminated water or soil. The infection has_symptom fever, has_symptom respiratory distress, has_symptom chest pain, and has_symptom stomach pain.]
obsolete recurrent childhood brainstem astrocytoma DOID_6385
obsolete recurrent childhood glioma of brain stem DOID_6382
childhood brain stem glioma DOID_6383
childhood brain stem neoplasm DOID_4206 [A brain stem cancer characterized by mass lesion of the brainstem in childhood, associated cranial nerve nuclei and long tracts, has_material_basis_in abnormally proliferating cells.]
obsolete primary Burkholderia infectious disease DOID_5053
adult cerebellar neoplasm DOID_5056
obsolete neuronal and mixed neuronal-glial tumor of cerebellum DOID_5055
childhood brainstem astrocytoma DOID_6386
rhabdoid meningioma DOID_5058
papillary meningioma of the cerebellum DOID_5057
Resentoviricetes NCBITaxon_2732459
Duplornaviricota NCBITaxon_2732405
spastic quadriplegic cerebral palsy 3 DOID_0081361 [A spastic quadriplegic cerebral palsy that has_material_basis_in homozygous mutation in the ADD3 gene on chromosome 10q24.]
spondyloepimetaphyseal dysplasia, Missouri type DOID_0080030 [A spondyloepimetaphyseal dysplasia that has_material_basis_in mutations in the MMP13 gene which results_in a pear-shaped vertebrae, abnormal metaphyseal changes, and genu varum deformities.]
childhood cerebellar neoplasm DOID_5059
fibrous dysplasia DOID_0080031 [A bone remodeling disease that results_in the destruction of normal bone and replacing it with fibrous bone tissue.]
Pierpont syndrome DOID_0081362 [An autosomal dominant intellectual developmental disorder that is characterized by distinctive facial characteristics, especially when smiling, plantar fat pads, and other limb anomalies and that has_material_basis_in heterozygous mutation in the TBL1XR1 gene on chromosome 3q26.]
distal myopathy with rimmed vacuoles DOID_0081363 [A distal myopathy that is characterized by adult onset of muscle weakness affecting the distal upper and lower limbs, which may result in walking difficulties, as well as proximal weakness of the shoulder girdle muscles and that has_material_basis_in by heterozygous mutation in the SQSTM1 gene on chromosome 5q35.]