Terminology Service < Semantic Lookup Platform

All terms in EFO

Label	Id	Description
HUES1	EFO_0005355	[A human embryonic stem cell line]
hermaphrodite gonad	UBERON_0002537	[A gonad with both testicular and ovarian aspects[WP].]
CAL120	EFO_0005356
hatching gland	UBERON_0002538	[The cells of the hatching gland contain enzymes responsible for solubilization of the egg chorion, facilitating the hatching process[GO]. A transversely oriented set of cells located deep to the EVL on the pericardial membrane, especially prominent during pharyngula period because of the brightly refractile cytoplasmic granules (containing hatching enzymes) of the principal cells of the gland.]
GM12801	EFO_0005353
milligram per kilogram body weight	EFO_0005354
obsolete_skin fragility-woolly hair-palmoplantar keratoderma syndrome	Orphanet_293165
encounter with health service for breast reconstruction following mastectomy	EFO_0020978	[Encounter with a health service for surgical reconstruction of the breast following mastectomy.]
CAL851	EFO_0005359
CAL148	EFO_0005357
CAL51	EFO_0005358
revision of total joint arthroplasty	EFO_0020974	[A surgical procedure of a joint in which some or all of the parts of the original prosthesis are removed and replaced for the purpose of correcting any problems that have developed since the initial surgery, such as aseptic loosening.]
total knee arthroplasty	EFO_0020975	[A surgical procedure in which the knee joint is replaced by a prosthetic implant.]
response to steroid	EFO_0020976	[Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of steroids.]
obsolete_infantile-onset ascending hereditary spastic paralysis	Orphanet_293168
occupational attainment	EFO_0020977	[A measure of occupational attainment through eg. hierarchical categorisation using the Standard Occupational Classification (SOC) system.]
deafness-oligodontia syndrome	MONDO_0009089	[Deafness-oligodontia syndrome is characterised by sensorineural hearing loss and oligodontia/hypodontia. It has been described in two pairs of siblings and in one isolated case. Dizziness was reported in one of the pairs of siblings. Transmission appears to be autosomal recessive.]
obsolete_congenital reticular ichthyosiform erythroderma	Orphanet_281190
nephrogenic diabetes insipidus-intracranial calcification syndrome	MONDO_0009099	[This syndrome is characterised by nephrogenic diabetes insipidus, intracerebral calcifications, intellectual deficit, short stature and facial dysmorphism.]
mucosulfatidosis	MONDO_0010088	[Multiple sulfatase deficiency (MSD) is a very rare and fatal lysosomal storage disease characterized by a clinical phenotype that combines the features of different sulfatase deficiencies (whether lysosomal or not) that can have neonatal (most severe), infantile (most common) and juvenile (rare) presentations with manifestations including hypotonia, coarse facial features, mild deafness, skeletal anomalies, ichthyosis, hepatomegaly, developmental delay, progressive neurologic deterioration and hydrocephalus.]