hasClinicalFeature
P190501
predicate
Indicates that an entity (such as a disease, condition, or case) exhibits or is characterized by a particular clinical sign, symptom, or feature.
Observed surface forms (2)
- hasCutaneousFeature ×5
- hasAutisticTraits ×1
Sample triples (75)
| Subject | Object |
|---|---|
| Elise Wassermann | true via predicate surface "hasAutisticTraits" ⓘ |
| MPS II | airway obstruction ⓘ |
| MPS II | behavioral problems ⓘ |
| MPS II | cardiac valve disease ⓘ |
| MPS II | cardiomyopathy ⓘ |
| MPS II | coarse facial features ⓘ |
| MPS II | dysostosis multiplex ⓘ |
| MPS II | hearing loss ⓘ |
| MPS II | hepatosplenomegaly ⓘ |
| MPS II | inguinal hernia ⓘ |
| MPS II | intellectual disability ⓘ |
| MPS II | joint stiffness ⓘ |
| MPS II | progressive developmental delay ⓘ |
| MPS II | recurrent ear infections ⓘ |
| MPS II | short stature ⓘ |
| MPS II | sleep apnea ⓘ |
| MPS II | spinal canal stenosis ⓘ |
| MPS II | umbilical hernia ⓘ |
| ORPHA:2382 | atonic seizures ⓘ |
| ORPHA:2382 | atypical absence seizures ⓘ |
| ORPHA:2382 | behavioral problems ⓘ |
| ORPHA:2382 | cognitive impairment ⓘ |
| ORPHA:2382 | developmental regression ⓘ |
| ORPHA:2382 | drop attacks ⓘ |
| ORPHA:2382 | drug-resistant epilepsy ⓘ |
| ORPHA:2382 | generalized tonic-clonic seizures ⓘ |
| ORPHA:2382 | intellectual disability ⓘ |
| ORPHA:2382 | multiple seizure types ⓘ |
| ORPHA:2382 | myoclonic seizures ⓘ |
| ORPHA:2382 | tonic seizures ⓘ |
| erythema nodosum | ankle swelling ⓘ |
| erythema nodosum | arthralgia ⓘ |
| erythema nodosum | bilateral lesions ⓘ |
| erythema nodosum | fever ⓘ |
| erythema nodosum | lesions that change color like bruises ⓘ |
| erythema nodosum | malaise ⓘ |
| erythema nodosum | nodules on the shins ⓘ |
| erythema nodosum | painful subcutaneous nodules ⓘ |
| erythema nodosum | symmetrical distribution ⓘ |
| erythema nodosum | tender red nodules ⓘ |
| light chain amyloidosis | arrhythmias ⓘ |
| light chain amyloidosis | constipation ⓘ |
| light chain amyloidosis | diarrhea ⓘ |
| light chain amyloidosis | fatigue ⓘ |
| light chain amyloidosis | heart failure with preserved ejection fraction ⓘ |
| light chain amyloidosis | hepatomegaly ⓘ |
| light chain amyloidosis | macroglossia ⓘ |
| light chain amyloidosis | malabsorption ⓘ |
| light chain amyloidosis | nephrotic syndrome ⓘ |
| light chain amyloidosis | orthostatic hypotension ⓘ |