Terminology Service < Semantic Lookup Platform

All terms in HP

Label	Id	Description
Abnormality of the gingiva	HP_0000168	[Any abnormality of the gingiva (also known as gums).]
Gingival fibromatosis	HP_0000169	[The presence of fibrosis of the gingiva.]
Abnormality of the dentition	HP_0000164	[Any abnormality of the teeth.]
Abnormality of the skeletal system	HP_0000924	[An abnormality of the skeletal system.]
Severe periodontitis	HP_0000166	[A severe form of periodontitis.]
Periodontitis	HP_0000704	[Inflammation of the periodontium.]
Narrow mouth	HP_0000160	[Distance between the commissures of the mouth more than 2 SD below the mean. Alternatively, an apparently decreased width of the oral aperture (subjective).]
Median cleft lip	HP_0000161	[A type of cleft lip presenting as a midline (median) gap in the upper lip.]
Abnormal oral morphology	HP_0031816	[Any structural anomaly of the mouth, which is also known as the oral cavity.]
Abnormality of von Willebrand factor	HP_0012146	[Decreased quantity or activity of von Willebrand factor. Von Willebrand factor mediates the adhesion of platelets to the collagen exposed on endothelial cell surfaces.]
Abnormality of the coagulation cascade	HP_0003256	[An abnormality of the coagulation cascade, which is comprised of the contact activation pathway (also known as the intrinsic pathway) and the tissue factor pathway (also known as the extrinsic pathway) as well as cofactors and regulators.]
Abnormality of multiple cell lineages in the bone marrow	HP_0012145
Abnormality monocyte morphology	HP_0012144	[Any structural anomaly of a myeloid mononuclear recirculating leukocyte that can act as a precursor of tissue macrophages, osteoclasts and some populations of tissue dendritic cells.]
Abnormal myeloid leukocyte morphology	HP_0010974	[An abnormality of myeloid leukocytes.]
Abnormal megakaryocyte morphology	HP_0012143	[Any structural anomaly of megakaryocytes. Mature blood platelets are released from the cytoplasm of megakaryocytes, which are bone-marrow resident cells.]
Bilineage myelodysplasia	HP_0012149	[Myelodysplasia with dysplastic changes in two of the myeloid lineages: erythroid, granulocytic, megakaryocytic.]
Multiple lineage myelodysplasia	HP_0012148	[Myelodysplasia with dysplastic changes in two or more of the myeloid lineages: erythroid, granulocytic, megakaryocytic.]
Reduced quantity of Von Willebrand factor	HP_0012147	[Decreased quantity of von Willebrand factor.]
Pancreatic squamous cell carcinoma	HP_0012142	[A subtype of ductal pancreatic carcinoma that is thought to originate from squamous metaplasia of pancreatic ductal epithelium.]
bicyclic compound	CHEBI_33636	[A molecule that features two fused rings.]