All terms in DOID

Label Id Description
angular cheilitis DOID_0060312 [A cheilitis characterized by inflammation of one or both of the corners of the mouth.]
cheilitis DOID_1762 [A lip disease characterized by the inflammation of the lips; which may include the perioral skin, the vermilion border and the labial mucosa.]
adenoid hypertrophy DOID_0060311 [An upper respiratory tract disease characterized by the unusual growth of the adenoid tonsil; has symptom snoring, has symptom hyponasality, has symptom otitis media with effusion, has symptom mouth breathing.]
episodic ataxia type 4 DOID_0050992 [An episodic ataxia that is characterized by vertigo and diplopia.]
clitoris UBERON_0002411
autonomic nervous system UBERON_0002410
cardiac arrest DOID_0060319 [A congestive heart failure characterized by a sudden stop in effective blood circulation due to the failure of the heart to contract effectively or at all.]
immune system UBERON_0002405
pericardium UBERON_0002407
episodic ataxia type 7 DOID_0050995 [An episodic ataxia that is characterized by episodes of weakness and dysarthria, and has_material_basis_in autosomal dominant inheritance.]
uvulitis DOID_0060310 [An upper respiratory tract disease characterized by the swelling of the uvula to 3-5 times its normal size.]
episodic ataxia type 6 DOID_0050994 [An episodic ataxia that is characterized by nystagmus and dysarthria, and has_material_basis_in autosomal dominant inheritance of mutation in the SLC1A3 gene.]
episodic ataxia type 8 DOID_0050996 [An episodic ataxia that is characterized by weakness, dysarthria and myokymia, and has_material_basis_in autosomal dominant inheritance of mutation in the UBR4 gene.]
autosomal recessive spinocerebellar ataxia 10 DOID_0050999 [An autosomal recessive cerebellar ataxia that is characterized by ataxia, dysarthria, nystagmus and marked cerebellar atrophy, has_material_basis_in mutation in the ANO10 gene.]
childhood absence epilepsy DOID_1825 [A childhood electroclinical syndrome that is characterized by brief and frequent absence seizures in children with age of onset between four and ten years.]
nonprogressive cerebellar ataxia with mental retardation DOID_0050998 [An autosomal dominant cerebellar ataxia that is characterized by early onset of nonprogressive cerebellar ataxia, developmental delay, intellectual impairment and cerebellar atrophy, and has_material_basis_in autosomal dominant inheritance of mutation in the CAMTA1 gene.]
status epilepticus DOID_1824
obsolete petit mal status DOID_1823
secondary lacrimal atrophy DOID_1822
Pneumocystis jirovecii NCBITaxon_42068