Terminology Service for NFDI4Health
All terms in DOID
| Label | Id | Description |
|---|---|---|
| distal limb integumentary appendage | UBERON_0009564 | |
| nasal cavity | UBERON_0001707 | |
| eyelash | UBERON_0001702 | |
| strand of hair | UBERON_0001037 | |
| jaw skeleton | UBERON_0001708 | |
| subdivision of skeleton | UBERON_0010912 | |
| Treponema pallidum | NCBITaxon_160 | |
| Treponema | NCBITaxon_157 | |
| Treponema pallidum subsp. pallidum | NCBITaxon_161 | |
| female reproductive system | UBERON_0000474 | |
| reproductive system | UBERON_0000990 | |
| testis | UBERON_0000473 | |
| gonad | UBERON_0000991 | |
| male reproductive organ | UBERON_0003135 | |
| Kufor-Rakeb syndrome | DOID_0060556 | [An early-onset Parkinson's disease that is characterized by supranuclear gaze palsy, spasticity, and dementia and has_material_basis_in homozygous or compound heterozygous mutation in a lysosomal type 5 ATPase encoding gene on chromosome 1p36.] |
| early-onset Parkinson's disease | DOID_0060894 | [A Parkinson's disease characterized by onset of motor symptoms early than typically seen, usually prior to 50 years of age.] |
| compound organ component | UBERON_0000471 | |
| multi-tissue structure | UBERON_0000481 | |
| ataxia with oculomotor apraxia type 3 | DOID_0060557 | |
| autosomal recessive cerebellar ataxia | DOID_0050950 | [A hereditary ataxia that has_material_basis_in autosomal recessive inheritance.] |