All terms in EFO
| Label | Id | Description |
|---|---|---|
| lymphoblastoid cell line | EFO_0005292 | |
| male | PATO_0000384 | [A biological sex quality inhering in an individual or a population whose sex organs contain only male gametes.] |
| HFFc6 | EFO_0009318 | [Human foreskin fibroblast cell line immortalized by infection with retroviral constrcuts that expressed the hTERT open reading frame] |
| fibroblast derived cell line | EFO_0002009 | |
| Homo sapiens cell line | EFO_0002888 | |
| obsolete_testis | EFO_0000984 | [A typically paired male reproductive gland that produces sperm and that in most mammals is contained within the scrotum at sexual maturity.] |
| obsolete_ejaculatory duct | EFO_0000985 | [Either of the paired ducts in the human male that are formed by the junction of the duct from the seminal vesicle with the vas deferens, pass through the prostate, and open into or close to the prostatic utricle.] |
| F123-CASTx129 | EFO_0009319 | [Immortalized mouse embryonic stem cell line] |
| mouse cell line | EFO_0002887 | [Cell lines derived from mice.] |
| obsolete_seminal vesicle | EFO_0000986 | [Either of a pair of glandular pouches that lie one on either side of the male reproductive tract and in the human male secrete a sugar- and protein-containing fluid into the ejaculatory duct.] |
| qualitative or quantitative defects of Torsin-1A-interacting protein 1 | MONDO_0018529 | |
| qualitative or quantitative protein defects in neuromuscular diseases | MONDO_0016139 | |
| Agenesis of cerebellar vermis | HP_0002335 | [Congenital absence of the vermis of cerebellum.] |
| Aplasia/Hypoplasia of the cerebellum | HP_0007360 | |
| congenital myopathy with myasthenic-like onset | MONDO_0018528 | [Congenital myopathy with myasthenic-like onset is a rare, genetic, non-dystrophic myopathy characterized by fatigable muscle weakness associated with congenital myopathy. Patients present with axial hypotonia, myopathic facies with fatigable ptosis, feeding difficulties, delayed gross motor development and proximal limb weakness with a RYR1-related typical pattern of muscle involvement (i.e. severe involvement of the soleus muscle and sparring of the rectus femoris, sartorius, gracilis and semitendinous muscles). Scoliosis and frequent respiratory tract infections are additional observed features.] |
| Prochlorococcus marinus subsp. pastoris str. CCMP1986 | NCBITaxon_59919 | |
| cosyntropin | CHEBI_3901 | [A synthetic peptide that is identical to the 24-amino acid segment at the N-terminal of adrenocorticotropic hormone (corticotropin). A segment similar in all species, it contains the biological activity that stimulates production of corticosteroids in the adrenal cortex. It is used diagnostically to investigate adrenocortical insufficiency.] |
| diagnostic agent | CHEBI_33295 | [A substance administered to aid diagnosis of a disease.] |
| tafenoquine | CHEBI_135752 | [A racemate comprising equimolar amounts of (R)- and (S)-tafenoquine.] |
| squamous cell carcinoma of pancreas | MONDO_0018521 | [A squamous cell carcinoma that involves the pancreas.] |