Terminology Service for NFDI4Health
All terms in EFO
| Label | Id | Description |
|---|---|---|
| obsolete_lung (Gallus gallus) | EFO_0003730 | |
| obsolete_lung (Macaca fascicularis) | EFO_0003732 | |
| obsolete_lung (Homo sapiens) | EFO_0003731 | |
| obsolete_lung (Rattus norvegicus) | EFO_0003734 | |
| obsolete_lung (Mus musculus) | EFO_0003733 | |
| obsolete_lung (Sus scrofa) | EFO_0003736 | |
| obsolete_lung (Rattus rattus) | EFO_0003735 | |
| pervasive developmental disorder - not otherwise specified | EFO_0003759 | [An autism spectrum disorder that involves some autistic symptoms occuring after age 3 with an abscence of all the traits necessary for a diagnosis of autism.] |
| obsolete_infantile Bartter syndrome with sensorineural deafness | Orphanet_89938 | |
| obsolete_autosomal dominant hypophosphatemic rickets | Orphanet_89937 | |
| X-linked hypophosphatemia | Orphanet_89936 | [X-linked hypophosphatemia (XLH) is a hereditary renal phosphate-wasting disorder characterized by hypophosphatemia, rickets and/or osteomalacia, and diminished growth.] |
| Mycobacterium tuberculosis | NCBITaxon_1773 | |
| Mycobacterium smegmatis | NCBITaxon_1772 | |
| Mycobacterium avium subsp. paratuberculosis | NCBITaxon_1770 | |
| obsolete_primary lipodystrophy | Orphanet_90970 | |
| central nervous system cyst | EFO_0003760 | [Congenital or acquired cysts of the brain, spinal cord, or meninges which may remain stable in size or undergo progressive enlargement., A congenital or acquired cyst that is present in the central nervous system.] |
| CAMA1 | EFO_0001100 | |
| vitamin D deficiency | EFO_0003762 | [A nutritional condition produced by a deficiency of VITAMIN D in the diet, insufficient production of vitamin D in the skin, inadequate absorption of vitamin D from the diet, or abnormal conversion of vitamin D to its bioactive metabolites. It is manifested clinically as RICKETS in children and OSTEOMALACIA in adults. (From Cecil Textbook of Medicine, 19th ed, p1406)] |
| CC531 | EFO_0001101 | |
| CFT-2 | EFO_0001102 |