All terms in DOID

Label Id Description
lice infestation DOID_5502 [A parasitic ectoparasitic infectious disease that involves infestation of lice, which are blood-feeding ectoparasitic insects of the order Phthiraptera.]
parasitic ectoparasitic infectious disease DOID_4110 [A parasitic infectious disease that is caused by organisms that live primarily on the surface of the host.]
Pediculus humanus capitis infestation DOID_5501 [A lice infestation that involves colonization of the hair and skin by the parasitic insect Pediculus humanus capitis, which feeds on blood several times daily and resides close to the scalp to maintain its body temperature. The symptoms include tickling feeling of something moving in the hair, itching, caused by an allergic reaction to louse saliva, and irritability.]
tanycytic ependymoma DOID_5504
obsolete recurrent anal cancer DOID_6835
papillary ependymoma DOID_5505
colon squamous cell carcinoma DOID_5519 [A squamous cell carcinoma that is located_in the colon.]
anterior segment dysgenesis 5 DOID_0080610 [An anterior segment dysgenesis that has_material_basis_in heterozygous mutation in the PAX6 gene on chromosome 11p13.]
anterior segment dysgenesis 6 DOID_0080611 [An anterior segment dysgenesis that has_material_basis_in compound heterozygous mutation in the CYP1B1 gene on chromosome 2p22.]
obsolete testicular intratubular germ cell neoplasia of the unclassified type DOID_6849 [A stage 0 cancer of the testis consisting of the uniform precursor of testicular germ cell tumors (GCTs). ITGCNU can be found in testicular tissue adjacent to GCTs in approximately 90 percent of adult cases and is found in all groups at risk for testicular cancer, including men with cryptorchid testes, prior testicular cancer, and individuals with abnormal sexual differentiation.]
anterior segment dysgenesis 7 DOID_0080612 [An anterior segment dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the PXDN gene on chromosome 2p25.]
osteoid UBERON_0008883
bone tissue UBERON_0002481
anterior segment dysgenesis 8 DOID_0080613 [An anterior segment dysgenesis that has_material_basis_in homozygous or compound heterozygous mutation in the CPAMD8 gene on chromosome 19p13.]
lymph node carcinoma DOID_0080618 [A lymph node cancer that has_material_basis_in abnormally proliferating cells derives_from epithelial cells.]
sensory organ benign neoplasm DOID_0060096 [A nervous system benign neoplasm that is located_in a sensory organ.]
oculocutaneous albinism type VI DOID_0080614 [An oculocutaneous albinism that has_material_basis_in an autosomal recessive null mutation of the SLC24A5 gene on chromosome 15q21.1.]
nephroma DOID_0080615 [A kidney benign neoplasm that is located_in the kidney cortex.]
lymph node benign neoplasm DOID_0080617 [An immune system organ benign neoplasm that is located_in the lymph nodes.]
obsolete glandular cell intraepithelial neoplasm DOID_6840