All terms in DOID
| Label | Id | Description |
|---|---|---|
| thymus basaloid carcinoma | DOID_7050 | |
| obsolete ectopic calcitonin production | DOID_8381 | |
| basaloid lung carcinoma | DOID_7045 | |
| obsolete mixed embryonal carcinoma and endodermal sinus neoplasm with seminoma of the testis | DOID_8376 | |
| ciliary body epithelioid cell melanoma | DOID_7042 | |
| uveal epithelioid cell melanoma | DOID_7040 | |
| obsolete metastatic vulvar cancer | DOID_7043 | |
| vulvar basaloid squamous cell carcinoma | DOID_7048 | [A vulva squamous cell carcinoma that is composed of nests of immature, basal-type squamous cells with scanty cytoplasm.] |
| autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5 | DOID_0111518 | [A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in RRM2B on chromosome 8q22.3.] |
| basaloid squamous cell skin carcinoma | DOID_7049 | |
| autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 6 | DOID_0111519 | [A chronic progressive external ophthalmoplegia characterized by muscle weakness, mainly affecting the lower limbs, external ophthalmoplegia, exercise intolerance and mtDNA deletions that has_material_basis_in heterozygous mutation in DNA2 on chromosome 10q21.3.] |
| cervical basaloid squamous cell carcinoma | DOID_7046 | [A cervical squamous cell carcinoma that is characterized by nests of immature, basal-type squamous cells with scanty cytoplasm.] |
| autosomal recessive progressive external ophthalmoplegia with mitochondrial DNA deletions 4 | DOID_0111516 | [A chronic progressive external ophthalmoplegia characterized by adult onset of eye muscle weakness and proximal limb muscle weakness that has_material_basis_in homozygous or compound heterozygous mutation in DGUOK on chromosome 2p13.1.] |
| penis basaloid carcinoma | DOID_7047 | |
| autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2 | DOID_0111517 | [A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in SLC25A4 on chromosome 4q35.1.] |
| thoracic cavity vein | UBERON_0003479 | |
| brain ventricle | UBERON_0004086 | |
| Li-Fraumeni syndrome 1 | DOID_0111503 | [A Li-Fraumeni syndrome that has_material_basis_in heterozygous mutation in TP53 on chromosome 17p13.1.] |
| obsolete mixed choriocarcinoma and seminoma of the testis | DOID_8390 | |
| pharyngoconjunctival fever | DOID_13801 | [A viral infectious disease that results in infection located in pharynx or located in conjunctiva, has_material_basis_in Human adenovirus 3 or has_material_basis_in Human adenovirus 7, which are transmitted by droplet spread of respiratory secretions or transmitted by fomites. The infection has symptom fever, has symptom lymphadenopathy of the neck, and has symptom headache.] |