Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
haplotype_block	SO_0000355	[A region of the genome which is co-inherited as the result of the lack of historic recombination within it.]
integron	SO_0000365	[A region encoding an integrase which acts at a site adjacent to it (attI_site) to insert DNA which must include but is not limited to an attC_site.]
quality_value	SO_0001686	[An experimental feature attribute that defines the quality of the feature in a quantitative way, such as a phred quality score.]
experimental_feature_attribute	SO_0001684	[An attribute of an experimentally derived feature.]
transposable_element_flanking_region	SO_0000364	[The region of sequence surrounding a transposable element.]
floxed_gene	SO_0000363	[A transgene that is floxed.]
obsolete ocular tuberculosis	DOID_233
invalidated_by_chimeric_cDNA	SO_0000362	[A cDNA clone constructed from more than one mRNA. Usually an experimental artifact.]
five_prime_restriction_enzyme_junction	SO_0001689	[The restriction enzyme cleavage junction on the 5' strand of the nucleotide sequence.]
FRT_flanked	SO_0000361	[An attribute to describe sequence that is flanked by the FLP recombinase recognition site, FRT.]
obsolete iridodialysis	DOID_239
obsolete adhesions and disruptions of iris and ciliary body	DOID_237
Joubert syndrome with orofaciodigital defect	DOID_0060376	[A Joubert syndrome that is characterized by orofaciodigital defect.]
orofaciodigital syndrome V	DOID_0060375	[An orofaciodigital syndrome that is characterized by postaxial polydactyly and median cleft of the upper lip and has_material_basis_in homozygous mutation in the DDX59 gene on chromosome 1q32.]
orofaciodigital syndrome IV	DOID_0060374	[An orofaciodigital syndrome that is characterized by dysmorphic facies, the development of harmartomas of the tongue, polydactyly and limb dysplasia, has_material_basis_in autosomal recessive inheritance of mutations in the TCTN3 gene.]
cannabis dependence	DOID_1849	[A drug dependence that involves the continued use of cannabis despite problems related to use of the substance.]
orofaciodigital syndrome III	DOID_0060373	[An orofaciodigital syndrome that is characterized by dysmorphic facies and severe intellectual deficits, and has_material_basis_in autosomal recessive inheritance.]
Parkinson's disease 15	DOID_0060372	[An early-onset Parkinson's disease that has_material_basis_in mutation in the FBXO7 gene on chromosome 22q12.3.]
Parkinson's disease 8	DOID_0060371	[A late onset Parkinson's disease that has_material_basis_in heterozygous mutation in the dardarin encoding gene on chromosome 12q12.]
lateral sclerosis	DOID_230	[A motor neuron disease characterized by painless but progressive weakness and stiffness of the muscles of the legs.]