All terms in EFO
| Label | Id | Description |
|---|---|---|
| small intestine primordium | FBbt_00005504 | |
| Drosophila embryonic structure | EFO_0003335 | |
| autosomal recessive spinocerebellar ataxia 14 | MONDO_0014159 | [Spectrin-associated autosomal recessive cerebellar ataxia is a rare, genetic neurological disease, due to SPTBN2 mutations, characterized by global development delay in infancy, followed by childhood-onset gait ataxia with limb dysmetria and dysdiadochokinesia, mild to severe intellectual disability, development of cerebellar atrophy, and abnormal eye movements (including a convergent squint, hypometric saccades, jerky pursuit movements and incomplete range of movement).] |
| dopamine agonist | CHEBI_51065 | [A drug that binds to and activates dopamine receptors.] |
| nephronophthisis 16 | MONDO_0014158 | [Any nephronophthisis in which the cause of the disease is a mutation in the ANKS6 gene.] |
| nephronophthisis | MONDO_0019005 | [Progressive tubulointerstitial injury, inherited in an autosomal recessive pattern, caused by mutations in genes involved in ciliary function, which may result in an end stage renal failure.] |
| rectum primordium | FBbt_00005506 | |
| mandibular hypoplasia-deafness-progeroid syndrome | MONDO_0014157 | |
| large intestine primordium | FBbt_00005505 | |
| Malpighian tubule main body primordium | FBbt_00005501 | |
| Micrococcus luteus | NCBITaxon_1270 | |
| obsolete_neuroferritinopathy | Orphanet_157846 | |
| mushroom body primordium | FBbt_00005508 | [Embryonic structure from which the mushroom body is derived. The development of the mushroom body proceeds as follows: axonogenesis of embryonic Kenyon cells starts late in embryonic stage 14. The axons from these cells extend towards the lateral protocerebral tract (LTP). During stage 16, a second set of Kenyon cell fibers form a second tract, closely apposed to the first. By late stage 16, both tracts extend anteriorly beyond the LTP to form the distal part of the peduncle. These tracts make a sharp medial turn close to the boundary with the deutocerebrum to form the medial lobe. By late stage 17 the vertical lobe has emerged as a collateral outgrowth from the point where these tracts bend. Finally, the calyx forms near to the end of embryogenesis.] |
| central brain primordium | FBbt_00005542 | [Primordium of the embryonic central brain in the extended germ band and dorsal closure embryo.] |
| embryonic central brain | FBbt_00005662 | [Brain of the embryo that excludes the optic lobes. It includes the protocerebrum, deutocerebrum and tritocerebrum.] |
| Charcot-Marie-Tooth disease recessive intermediate C | MONDO_0014154 | [Autosomal recessive intermediate Charcot-Marie-Tooth disease type C is a rare subtype of autosomal recessive intermediate Charcot-Marie-Tooth (CMT) disease characterized by childhood to adulthood-onset of progressive, moderate to severe, predominantly distal, mostly lower limb muscle weakness and atrophy, foot deformities (including pes cavus and hammer toes), absent deep tendon reflexes and distal sensory loss associated with decreased motor and sensory nerve conduction velocities and features of both demyelinating and axonal neuropathy on sural nerve biopsy.] |
| autosomal recessive intermediate Charcot-Marie-Tooth disease | MONDO_0017058 | [Autosomal recessive form of intermediate Charcot-Marie-Tooth disease.] |
| Ruminococcus flavefaciens | NCBITaxon_1265 | |
| potassium nitrate | CHEBI_63043 | |
| callus formation | GO_1990110 | [ The process by which a callus is formed at a wound site. A plant callus is a portion of plant tissue that consists of mass of undifferentiated plant cells. It consists primarily of parenchyma cells but possibly contains other cell types as the callus begins to differentiate. ] |