All terms in DOID

Label Id Description
medulla of organ UBERON_0000958
Scedosporium boydii NCBITaxon_5597
Scedosporium NCBITaxon_41687
chromosome 6q24-q25 deletion syndrome DOID_0060424 [A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 6q24-q25 region.]
chromosome 8q21.11 deletion syndrome DOID_0060425 [A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 8q21.11 region and that is characterized by intellectual disability and common facial dysmorphic features.]
chromosome 19p13.13 deletion syndrome DOID_0060426 [A chromosomal deletion syndrome that has_material_basis_in a chromosome 19p13.13 deletion and that is characterized by an unusually large head size, tall stature, and intellectual disability that is usually moderate in severity.]
chromosome Xp21 deletion syndrome DOID_0060427 [A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome Xp21 region.]
flexor muscle UBERON_0000366
Microascaceae NCBITaxon_5593
Microascales NCBITaxon_5592
SATB2-associated syndrome DOID_0060428 [A syndrome that has_material_basis_in genetic changes that affect the SATB2 gene and that is characterized by mild to severe intellectual disability, a delayed or absent ability to speak, severe speech anomalies, abnormalities of the palate, teeth anomalies, behavioral issues with or without bone or brain anomalies, and onset before age 2.]
Hypocreomycetidae NCBITaxon_222543
Rhinocladiella NCBITaxon_5587
chromosome 4q21 deletion syndrome DOID_0060420 [A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 4q21 region.]
broad ligament of uterus UBERON_0012332
ligament UBERON_0000211
cranial cartilage UBERON_0003933
perianal skin UBERON_0012336
skin of pelvis UBERON_0001415
subepithelial mucinous corneal dystrophy DOID_0060454 [An epithelial and subepithelial dystrophy that is characterized by frequent, recurrent corneal erosions in the first decade of life.]