Terminology Service for NFDI4Health
All terms in EFO
| Label | Id | Description |
|---|---|---|
| obsolete_X-linked ichthyosis syndrome | Orphanet_281210 | |
| obsolete_autosomal ichthyosis syndrome | Orphanet_281217 | |
| mesonephros | UBERON_0000080 | [The second stage of the kidney. It serves as the main excretory organ of aquatic vertebrates and as a temporary embryonic kidney in higher vertebrates. It is composed of the mesonephric duct (also called the Wolffian duct), mesonephric tubules, and associated capillary tufts. A single tubule and its associated capillary tuft is called a mesonephric excretory unit; these units are similar in structure and function to nephrons of the adult kidney. The mesonephros is derived from intermediate mesoderm in the vertebrate embryo.] |
| hypoblast (generic) | UBERON_0000089 | |
| inner cell mass | UBERON_0000087 | [A mass of cells that develop into the body of the embryo and some extraembryonic tissues.] |
| embryonic cell (metazoa) | CL_0002321 | [A cell of the embryo.] |
| Autosomal ichthyosis syndrome with prominent hair abnormalities | Orphanet_281222 | |
| Gerbera hybrid cultivar | NCBITaxon_18101 | |
| obsolete_mosaic genome-wide paternal uniparental disomy | Orphanet_329813 | |
| Congenital cataracts - facial dysmorphism - neuropathy | Orphanet_48431 | |
| Cerebral disease with cataract | Orphanet_98645 | |
| Familial transthyretin-related amyloidosis | Orphanet_271861 | |
| Vibrio alginolyticus | NCBITaxon_663 | |
| caudal tuberal nucleus | UBERON_2000482 | |
| Vibrio cholerae | NCBITaxon_666 | |
| 5p13 microduplication syndrome | Orphanet_329802 | |
| Multiple prenatal fractures | HP_0005855 | [The presence of bone fractures in the prenatal period that are diagnosed at birth or before.] |
| obsolete_genetic cardiac anomaly | Orphanet_271853 | |
| Vibrio parahaemolyticus | NCBITaxon_670 | |
| Autosomal ichthyosis syndrome with fatal disease course | Orphanet_281241 |