Terminology Service for NFDI4Health
All individuals in ICD10
| Label | Id | Description |
|---|---|---|
| Retinal detachment with retinal break | H33.0 | |
| Retinal detachments and breaks | H33 | |
| Retinal disorder, unspecified | H35.9 | |
| Retinal disorders in diseases classified elsewhere | H36 | |
| Retinal haemorrhage | H35.6 | |
| Retinal vascular occlusion, unspecified | H34.9 | |
| Retinal vascular occlusions | H34 | |
| Retinopathy of prematurity | H35.1 | |
| Retinoschisis and retinal cysts | H33.1 | |
| Retracted nipple associated with childbirth | O92.0 | |
| Retrobulbar neuritis in diseases classified elsewhere | H48.1 | |
| Retrograde amnesia | R41.2 | |
| Retropharyngeal and parapharyngeal abscess | J39.0 | |
| Retrovirus as the cause of diseases classified to other chapters | B97.3 | |
| Retrovirus infections, not elsewhere classified | B33.3 | |
| Rett's syndrome | F84.2 | [A condition, so far found only in girls, in which apparently normal early development is followed by partial or complete loss of speech and of skills in locomotion and use of hands, together with deceleration in head growth, usually with an onset between seven and 24 months of age. Loss of purposive hand movements, hand-wringing stereotypies, and hyperventilation are characteristic. Social and play development are arrested but social interest tends to be maintained. Trunk ataxia and apraxia start to develop by age four years and choreoathetoid movements frequently follow. Severe mental retardation almost invariably results.] |
| Reye's syndrome | G93.7 | |
| Rh incompatibility reaction | T80.4 | |
| Rh isoimmunization of fetus and newborn | P55.0 | |
| Rheumatic aortic insufficiency | I06.1 |