Terminology Service for NFDI4Health
All terms in SNOMED
| Label | Id | Description |
|---|---|---|
| Peroxidase (disposition) | 736210002 | |
| Malignant tumor involving vagina by separate metastasis from uterus (disorder) | 369586001 | |
| Succinate cytochrome C reductase (substance) | 708051001 | |
| Marshallagia orientalis (organism) | 14186006 | |
| Primary hybrid total knee replacement (procedure) | 450818008 | |
| Chest lead (physical object) | 257483001 | |
| Ribonucleic acid of Influenza A virus H1 (substance) | 707903009 | |
| Proximal symphalangism of bilateral fingers (disorder) | 890425005 | |
| Traumatic alopecia (disorder) | 67488005 | |
| Fascia of hand drained (situation) | 287910005 | |
| Part III accommodation arranged (finding) | 160731008 | |
| Product containing becaplermin in cutaneous dose form (medicinal product form) | 772326009 | |
| Fatal X-linked ataxia with deafness and loss of vision (disorder) | 702441001 | [Syndrome with characteristics of intellectual deficit, early-onset hypotonia, ataxia, delayed motor development, hearing impairment and loss of vision due to optic atrophy. Other manifestations included floppiness, susceptibility to infections and later flaccid tetraplegia and areflexia. It is caused by missense mutations in the phosphoribosyl pyrophosphate synthetase 1 gene (PRPS1) localised to Xq22.1-q24, leading to impaired purine biosynthesis. Transmitted as an X-linked recessive trait. The disease has a fatal course during childhood (the majority of patients die before the age of 5 years) due to the high susceptibility of the patients to infections, especially of the upper respiratory tract., Syndrome with characteristics of intellectual deficit, early-onset hypotonia, ataxia, delayed motor development, hearing impairment and loss of vision due to optic atrophy. Other manifestations included floppiness, susceptibility to infections and later flaccid tetraplegia and areflexia. It is caused by missense mutations in the phosphoribosyl pyrophosphate synthetase 1 gene (PRPS1) localized to Xq22.1-q24, leading to impaired purine biosynthesis. Transmitted as an X-linked recessive trait. The disease has a fatal course during childhood (the majority of patients die before the age of 5 years) due to the high susceptibility of the patients to infections, especially of the upper respiratory tract.] |
| Victim of abusive sexual relationship with partner (finding) | 418150003 | |
| Microscopic examination of bacterial smear of specimen from integument (procedure) | 608968004 | |
| Barotitis externa (disorder) | 241980009 | |
| Crystal violet tattoo (finding) | 840342004 | |
| Abdominal weakness (finding) | 162239000 | |
| Posterior cord syndrome of spinal cord at eighth cervical level (disorder) | 721397006 | |
| Carcinoma of glottis (disorder) | 372103002 |