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obsolete Linear Eccrine nevus with Comedones
|
DOID_6851 |
|
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head and neck squamous cell carcinoma
|
DOID_5520 |
[A head and neck carcinoma that has_material_basis_in squamous cells that line the moist, mucosal surfaces inside the head and neck.] |
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head and neck carcinoma
|
DOID_1542 |
[A head and neck cancer that has_material_basis_in epithelial cells and is located in the upper aerodigestive tract, including the lip, oral cavity (mouth), nasal cavity, paranasal sinuses, pharynx, and larynx.] |
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ethmoid sinus ectopic meningioma
|
DOID_6854 |
|
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ethmoidal sinus benign neoplasm
|
DOID_1364 |
|
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basaloid squamous cell carcinoma
|
DOID_5522 |
[A squamous cell carcinoma that has a solid, closely packed growth of cells with hyperchromatic nuclei, scant cytoplasm, small cystic spaces, and foci of necrosis. It has overlying squamous dysplasia, rare foci of overt keratinization, and/or coexistent keratinizing squamous cell carcinoma.] |
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keratinizing squamous cell carcinoma
|
DOID_5521 |
[A squamous cell carcinoma that presents as single, isolated cells with bizarre cytoplasmic shapes, intense cytoplasmic eosinophilia, and intensely hyperchromatic, angular nuclei in a background of necrotic and keratinous debris.] |
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obsolete eccrine angiomatous hamartoma
|
DOID_6852 |
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adenoid squamous cell carcinoma
|
DOID_5524 |
[A squamous cell carcinoma that is characterized by a tubular microscopic pattern and keratinocyte acantholysis.] |
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pineal region immature teratoma
|
DOID_6858 |
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pineal region teratoma
|
DOID_6856 |
|
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middle ear squamous cell carcinoma
|
DOID_5526 |
[A middle ear carcinoma that has_material_basis_in squamous cells.] |
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anal squamous cell carcinoma
|
DOID_5525 |
[An anal carcinoma that arises near the squamocolumnar junction.] |
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pineal region mature teratoma
|
DOID_6857 |
[A mature teratoma that is located_in the pineal region.] |
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ampulla of Vater squamous cell carcinoma
|
DOID_5527 |
[An ampulla of Vater carcinoma that derives_from epithelial squamous cells.] |
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Fazio-Londe disease
|
DOID_0080632 |
[A progressive bulbar palsy that is characterized by motor, sensory and cranial neuronopathy and that has_material_basis_in homozygous mutation in the C20ORF54 gene on chromosome 20p13.] |
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progressive bulbar palsy
|
DOID_681 |
|
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brainstem intraparenchymal clear cell meningioma
|
DOID_4209 |
|
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developmental cardiac valvular defect
|
DOID_0080633 |
[A physical disorder that has_material_basis_in homozygous or compound heterozygous mutation in the PLD1 gene on chromosome 3q26.] |
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nanophthalmos
|
DOID_0080634 |
[A microphthalmia that is characterized by a small eye with a short axial length, severe hyperopia, an elevated lens/eye ratio, and a high incidence of angle-closure glaucoma.] |