Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
acute enteritis	SYMP_0000676	[Acute enteritis is a enteritis with either or both a rapid onset and a short course which is usually due to bacteria or virus.]
neurofibromatosis	DOID_8712
bradykinesia	SYMP_0000673	[Bradykinesia is a hypokinesia characterized by an extreme slowness in the execution of movements and reflexes.]
acute cranial nerve dysfunction	SYMP_0000674
obsolete carcinoma in situ of respiratory system	DOID_8718	[A carcinoma in situ that is characterized by the spread of cancer in the respiratory system and the lack of invasion of surrounding tissues.]
sudden onset of fever	SYMP_0000671
decubitus ulcer	DOID_8717	[Decubitus ulcer is a chronic ulcer of skin where the ulcer is an ulceration of tissue deprived of adequate blood supply by prolonged pressure.]
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 GUCA1A on chromosome 6p21.1.]
cone-rod dystrophy	DOID_0050572	[A retinal degeneration that characterized by progressive deterioration of the cone and rod photoreceptor cells.]
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 MLC1 on chromosome 22q13.]
circling movement	SYMP_0000688
X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance	DOID_0080311	[A syndromic X-linked intellectual disability characterized by neonatal hypotonia with motor delay but no obvious ataxia, marked strabismus, early-onset complex partial seizures, and moderate to severe mental retardation and has_material_basis_in mutation in the oligophrenin-1 gene.]
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 ARHGEF2 on chromosome 1q22.]
Poeae Chloroplast Group 2 (Poeae type)	NCBITaxon_1652081