All terms in EFO
| Label | Id | Description |
|---|---|---|
| Reticulocyte Corpuscular Hemoglobin Content | EFO_0009229 | [The determination of the amount of hemoglobin in reticulocytes within a sample. [ NCI ]] |
| obsolete_enteric nervous system | EFO_0000895 | [Two ganglionated neural plexuses in the gut wall which form one of the three major divisions of the autonomic nervous system. The enteric nervous system innervates the gastrointestinal tract, the pancreas, and the gallbladder. It contains sensory neurons, interneurons, and motor neurons. Thus the circuitry can autonomously sense the tension and the chemical environment in the gut and regulate blood vessel tone, motility, secretions, and fluid transport. The system is itself governed by the central nervous system and receives both parasympathetic and sympathetic innervation.] |
| obsolete_EEC syndrome | Orphanet_1896 | [EEC syndrome is a genetic developmental disorder characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip/palate).] |
| obsolete_ventral nerve cord | EFO_0000896 | [The pair of closely united ventral longitudinal nerves with their segmental ganglia that is characteristic of many elongate invertebrates (as earthworms).] |
| obsolete_EEM syndrome | Orphanet_1897 | |
| pharyngeal nervous system | EFO_0000897 | |
| obsolete_somatic nervous system | EFO_0000898 | |
| O-3-methylglutarylcarnitine | CHEBI_70857 | [An O-methylglutarylcarnitine compound having 3-methylglutaryl as the acyl substituent.] |
| obsolete_autopod | EFO_0000877 | |
| autosomal recessive spastic paraplegia type 67 | MONDO_0018419 | [Autosomal recessive spastic paraplegia type 67 is an extremely rare, complex hereditary spastic paraplegia characterized by an infancy or childhood onset of global developmental delay and progressive spasticity with tremor in the distal limbs, increased deep tendon reflexes and extensor plantar responses, which may be associated with mild intellectual disability. Additional features include muscle wasting and cerebellar abnormalities.] |
| obsolete_zeugopod | EFO_0000878 | [The middle part of the limb (e.g. between the elbow and wrist)] |
| autosomal recessive spastic paraplegia type 66 | MONDO_0018418 | |
| obsolete_stylopod | EFO_0000879 | [The proximal part of the limb (e.g. between shoulder and elbow)] |
| Respiratory failure requiring assisted ventilation | HP_0004887 | [A state of respiratory distress that requires a life saving intervention in the form of gaining airway access and instituting positive pressure ventilation.] |
| Respiratory insufficiency | HP_0002093 | |
| Absent axillary hair | HP_0002221 | [Absence of axillary hair.] |
| autosomal recessive spastic paraplegia type 60 | MONDO_0018417 | |
| autosomal recessive spastic paraplegia type 59 | MONDO_0018416 | |
| obsolete rare female infertility due to hypothalamic-pituitary-gonadal axis disorder of genetic origin | MONDO_0018411 | [OBSOLETE. An instance of rare female infertility due to hypothalamic-pituitary-gonadal axis disorder that is caused by a modification of the individual's genome.] |
| obsolete female infertility due to an anomaly of ovarian function of genetic origin | MONDO_0018413 |