Terminology Service < Semantic Lookup Platform

All terms in HP

Label	Id	Description
Focal cortical dysplasia type II	HP_0032051	[A type of focal cortical dysplasia that is characterized by disrupted cortical lamination and specific cytological abnormalities.]
Focal cortical dysplasia type Ic	HP_0032050	[A subtype of focal cortical dysplasia type I that is characterized by abnormal radial and tangential cortical lamination.]
Mild malformation of cortical development	HP_0032059	[A malformation of cortical development characterized by mild abnormalities of the cortex: excessive heterotopic neurons in Layer 1 or microscopic neuronal clusters or excess of single neurons of normal morphology in deep white matter.]
Focal cortical dysplasia type IIId	HP_0032058	[A subtype of focal cortical dysplasia type III that is characterized by altered architectural (cortical dyslamination, hypoplasia without six-layered structure) or cytoarchitectural composition (hypertrophic neurons) of the neocortex, which occur adjacent to other lesions acquired during early life (not included into FCD Type IIIa-c). These lesions comprise a large spectrum including traumatic brain injury, glial scarring after prenatal or perinatal ischemic injury or bleeding, and inflammatory or infectious diseases, i.e. Rasmussen encephalitis, limbic encephalitis, bacterial or viral infections.]
Focal cortical dysplasia type III	HP_0032054	[A type of focal cortical dysplasia that is characterized by cortical lamination abnormalities associated with a principal lesion, usually adjacent to or affecting the same cortical area/lobe.]
Focal cortical dysplasia type IIIc	HP_0032057	[A subtype of focal cortical dysplasia type III that is characterized by alterations in architectural (cortical dyslamination, hypoplasia) or cytoarchitectural composition of the neocortex (hypertrophic neurons), which occur adjacent to vascular malformations (cavernomas, arteriovenous malformations, leptomeningeal vascular malformations, telangiectasias, meningioangiomatosis).]
Focal cortical dysplasia type IIIb	HP_0032056	[A subtype of focal cortical dysplasia type III that is characterized by altered architectural (cortical dyslamination, hypoplasia without six-layered structure) and/or cytoarchitectural composition (hypertrophic neurons) of the neocortex, which occur adjacent to glial or glioneuronal tumor.]
Focal cortical dysplasia type IIIa	HP_0032055	[A subtype of focal cortical dysplasia type III that is characterized by alterations in architectural organisation (cortical dyslamination) or cytoarchitectural composition (hypertrophic neurons outside Layer 5) in patients with hippocampal sclerosis (HS, syn. Ammon's horn sclerosis).]
Focal cortical dysplasia type IIb	HP_0032053	[A subtype of focal cortical dysplasia type II that is characterized by dysmorphic neurons (significantly enlarged with accumulation of neurofilament proteins) and balloon cells.]
pectinate line	UBERON_0006574	[The pectinate line (anocutaneous line, dentate line, anorectal junction) is a line which divides the upper 2/3rds and lower 1/3rd of the anal canal. Developmentally, this line represents the hindgut-proctodeum junction. It is an important anatomical landmark, and several distinctions can be made based upon the location of a structure relative to this line:]
DNA nucleotidylexotransferase (human)	PR_P04053	[A DNA nucleotidylexotransferase that is encoded in the genome of human.]
DNA nucleotidylexotransferase	PR_000006611	[A protein that is a translation product of the human DNTT gene or a 1:1 ortholog thereof.]
lower secondary canine tooth	UBERON_0018562	[A secondary canine tooth that is part of a lower jaw region.]
secondary canine tooth	UBERON_0018584
upper secondary canine tooth	UBERON_0018561	[A secondary canine tooth that is part of a upper jaw region.]
lower central secondary incisor tooth	UBERON_0018568	[A lower jaw incisor that is in_the_central_side_of a dentition.]
vestibular system	UBERON_0004681	[The sensory system for the sense of balance.]
alkaline phosphatase, placental type, signal peptide removed form (human)	PR_000046326	[An alkaline phosphatase, placental type (human) that has had the signal peptide removed. UniProtKB:P05187, 23-535.]
alkaline phosphatase, placental type, signal peptide removed form	PR_000018968	[An alkaline phosphatase, placental type that has had the signal peptide removed.]
alkaline phosphatase, placental type (human)	PR_P05187	[An alkaline phosphatase, placental type that is encoded in the genome of human.]