Terminology Service < Semantic Lookup Platform

All terms in DOID

Label	Id	Description
obsolete flat adenoma syndrome	DOID_5687
acinar cell carcinoma	DOID_3025	[A carcinoma that has_material_basis_in abnormally proliferating cells, derives_from spindle cells and/or derives_from giant cells.]
acinar cell	CL_0000622
obsolete metastatic prostatic adenocarcinoma	DOID_3026
obsolete metastatic melanoma	DOID_4358
obsolete experimental melanoma	DOID_4357
Werner syndrome	DOID_5688	[A syndrome characterized by premature aging and age-related phenotypes such as atherosclerosis, arteriosclerosis, cataracts, osteoporosis, soft tissue calcification, premature thinning, graying, and loss of hair, as well as a high incidence of some types of cancers and that has_material_basis_in mutations in the WRN gene, on chromosome 8.]
obsolete metastatic adenocarcinoma	DOID_3027
obsolete intramucosal adenocarcinoma colon adenoma	DOID_3028
Hexamitidae	NCBITaxon_5739
Diplomonadida	NCBITaxon_5738
amelanotic melanoma	DOID_4359
colon mucinous adenocarcinoma	DOID_3029
colon adenocarcinoma	DOID_234	[A colon carcinoma that derives_from epithelial cells of glandular origin.]
mucinous adenocarcinoma	DOID_3030	[An adenocarcinoma that derives_from epithelial cells originating in glandular tissue, which produce mucin.]
Fornicata	NCBITaxon_207245
NGLY1-deficiency	DOID_0060728	[A carbohydrate metabolic disorder that is characterized by global developmental delay, hypotonia, abnormal involuntary movements, and alacrima or poor tear production and that has_material_basis_in homozygous or compound heterozygous mutation in the NGLY1 gene on chromosome 1p24.]
carbohydrate metabolic disorder	DOID_2978	[An inherited metabolic disorder that affect the catabolism and anabolism of carbohydrates.]
Acanthomorphata	NCBITaxon_123368
autosomal recessive congenital ichthyosis 11	DOID_0060720	[An autosomal recessive congenital ichthyosis characterized by ichthyosis, hypotrichosis, photophobia, corneal opacity, pingueculum, blepharitis, marked acanthosis, otrhohyperkeratosis and hyperkeratosis that has_material_basis_in homozygous mutation in the ST14 gene on chromosome 11q24.]