All terms in EFO
| Label | Id | Description |
|---|---|---|
| all-cis-icosa-8,11,14-trienoic acid | CHEBI_53486 | [An icosatrienoic acid having three cis double bonds at positions 8, 11 and 14.] |
| Populus nigra | NCBITaxon_3691 | |
| Populus tremuloides | NCBITaxon_3693 | |
| Populus trichocarpa | NCBITaxon_3694 | |
| obsolete class I glucose-6-phosphate dehydrogenase deficiency | MONDO_0018750 | |
| Populus | NCBITaxon_3689 | |
| esophageal small cell neuroendocrine carcinoma | MONDO_0004116 | [An aggressive, high-grade and poorly differentiated carcinoma with neuroendocrine differentiation that arises from the esophagus. It is characterized by the presence of malignant small cells.] |
| esophageal neuroendocrine tumor | MONDO_0003649 | [A well differentiated, low or intermediate grade tumor with neuroendocrine differentiation that arises from the esophagus.] |
| refractory hematologic cancer | MONDO_0004111 | [A hematologic malignancy that is resistant to treatment.] |
| increased rate | PATO_0000912 | [A rate which is relatively high.] |
| obsolete glycogen storage disease VIII | MONDO_0006772 | |
| obsolete_commissural facial cleft | Orphanet_141276 | |
| idiopathic cardiomyopathy | EFO_0000767 | [A disease of the heart muscle or myocardium proper whose cause is unknown.] |
| idiopathic pulmonary fibrosis | EFO_0000768 | [Idiopathic pulmonary fibrosis (IPF) is a nonneoplastic pulmonary disease that is characterized by the formation of scar tissue within the lungs in the absence of any known cause.] |
| Human herpesvirus 4 | NCBITaxon_10376 | |
| obsolete_peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome | Orphanet_397744 | |
| acquired skeletal muscle disease | MONDO_0016105 | [An instance of skeletal muscle disease that is acquired during the lifetime of the individual.] |
| progressive muscular dystrophy | MONDO_0016106 | |
| myotonic dystrophy | MONDO_0016107 | [An inherited progressive disorder affecting the muscles. It is characterized by muscle wasting and hypotonia, cataracts, heart conduction defects and endocrinopathies.] |
| familial cold autoinflammatory syndrome | MONDO_0018768 | [Familial cold urticaria (FCAS) is the mildest form of cryopyrin-associated periodic syndrome (CAPS) and is characterized by recurrent episodes of urticaria-like skin rash triggered by exposure to cold associated with low-grade fever, general malaise, eye redness and arthralgia/myalgia.] |