Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
Limitation of neck motion	HP_0005986
Progressive muscle weakness	HP_0003323
obsolete insect visual anlage in statu nascendi	UBERON_6005425
Ivemark syndrome	Orphanet_97548
obsolete_sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy	Orphanet_97555
Congenital and infantile nephrotic syndrome	Orphanet_97556
Aristolochia fimbriata	NCBITaxon_158543
non-syndromic intellectual disability	MONDO_0000509	[An intellectual disability that is not part of a larger syndrome.]
inclusion body myopathy with Paget disease of bone and frontotemporal dementia	MONDO_0000507	[Inclusion body myopathy with Paget disease of bone and frontotemporal dementia (IBMPFD) is a multisystem degenerative genetic disorder characterized by adult-onset proximal and distal muscle weakness (clinically resembling limb-girdle muscular dystrophy); early-onset Paget disease of bone, manifesting with bone pain, deformity and enlargement of the long-bones; and premature frontotemporal dementia, manifesting first with dysnomia, dyscalculia and comprehension deficits followed by progressive aphasia, alexia, and agraphia. As the disease progresses, muscle weakness begins to affect the other limbs and respiratory muscles, ultimately resulting in respiratory or cardiac failure.]
Polymenorrhea	HP_0400007	[Frequent menses; menstrual cycles lasting less than 21 days.]
insect anlage in statu nascendi	UBERON_6005413	['anlagen in statu nascendi' are domains that do not yet coincide 1:1 with a later organ. Anlagen in statu nascendi are typically defined for the early blastoderm by the expression domains of genes which, in the late blastoderm or later, are expressed in specific anlagen, but initially come on in larger domains.]
Neisseria meningitidis MC58	NCBITaxon_122586
acetyltaurine	CHEBI_84415	[An amino sulfonic acid that is taurine substituted by an acetyl group at the N atom.]
normophosphatemic familial tumoral calcinosis	MONDO_0012502
thiopurine S-methyltransferase deficiency	MONDO_0012503	[An acquired metabolic disease that is has its basis in the disruption of thiopurine S-methyltransferase activity.]
bone squamous cell carcinoma	MONDO_0000514	[A squamous cell carcinoma that involves the bone tissue.]
late cleavage stage embryo Ce	EFO_0005502	[C. elegans 210-350min after first cleavage at 20 Centigrade. Proliferate from 421 cells to 560 cells. The stage before the fast cleavage of cells finishes.]
proliferating embryo Ce	EFO_0005501	[C. elegans 0-350min after first cleavage at 20 Centigrade. Proliferate from 1 cell to 560 cells. From start of first cleavage till cleavage is over.]
gastrulating embryo Ce	EFO_0005503	[C. elegans 100-290min after first cleavage at 20 Centigrade. Proliferate from 28 cells to 421 cells. Referring to the whole period of gastrulation.]
4-cell embryo Ce	EFO_0005500	[C. elegans 20-40min after first cleavage at 20 Centigrade. Contains 4 cells.]