Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
speech disorder	DOID_92	[A communication disorder that involves difficulty with the act of speech production.]
language disorder	DOID_93	[A communication disorder that involves the processing of linguistic information.]
degenerative disc disease	DOID_90	[A bone deterioration disease that has_material_basis_in gradual dehydration and tears located_in intervertebral disc.]
bone deterioration disease	DOID_0080007	[A bone structure disease that results_in change or damage of structure located_in bone.]
rectorrhagia	SYMP_0000639
opisthotonus	SYMP_0000637
papular rash	SYMP_0000638
low backache	SYMP_0000635
maculopapular rash	SYMP_0000636
inflammatory low back pain	SYMP_0000633
leukocytosis	SYMP_0000634
multiple epiphyseal dysplasia due to collagen 9 anomaly	DOID_0070305	[A multiple epiphyseal dysplasia that has_material_basis_in mutation in any of the members of the COL9A gene family (COL9A1, COL9A2, COL9A3).]
multiple epiphyseal dysplasia	DOID_12721	[An osteochondrodysplasia that has_material_basis_in defective cartilage mineralization into bone which results in irregular ossification centers of the located in hip or located in knee. The disease has symptom fatigue, has symptom joint pain.]
post-cardiac arrest syndrome	DOID_0070306	[A syndrome that is characterized by four main components: post-cardiac arrest brain injury, post-cardiac arrest myocardial dysfunction, systemic ischemia reperfusion response, and persistent precipitating pathologies.]
multiple epiphyseal dysplasia 1	DOID_0070303	[A multiple epiphyseal dysplasia that has_material_basis_in heterozygous mutation in the COMP gene on chromosome 19p13.]
multiple epiphyseal dysplasia 3	DOID_0070304	[A multiple epiphyseal dysplasia due to collagen 9 anomaly that has_material_basis_in heterozygous mutation in the COL9A3 gene on chromosome 20q13.]
multiple epiphyseal dysplasia 6	DOID_0070301	[A multiple epiphyseal dysplasia due to collagen 9 anomaly that has_material_basis_in heterozygous mutation in the COL9A1 gene on chromosome 6p13.]
multiple epiphyseal dysplasia 7	DOID_0070302	[A multiple epiphyseal dysplasia that has_material_basis_in homozygous mutation in the CANT1 gene on chromosome 17q25.]
tract of diencephalon	UBERON_0011591
tract of brain	UBERON_0007702