All terms in MONDO
| Label | Id | Description |
|---|---|---|
| severe primary trimethylaminuria | MONDO_0018767 | |
| chronic enteropathy associated with SLCO2A1 gene | MONDO_0018766 | |
| isosporiasis | MONDO_0018769 | |
| familial cold autoinflammatory syndrome | MONDO_0018768 | |
| rippling muscle disease with myasthenia gravis | MONDO_0016100 | |
| acquired rippling muscle disease | MONDO_0021142 | |
| tubulinopathy-associated dysgyria | MONDO_0018763 | |
| neurolymphomatosis | MONDO_0016101 | |
| cryptogenic multifocal ulcerous stenosing enteritis | MONDO_0018765 | |
| subacute inflammatory demyelinating polyneuropathy | MONDO_0016102 | |
| isolated asymptomatic elevation of creatine phosphokinase | MONDO_0016103 | |
| caveolinopathy | MONDO_0016146 | |
| qualitative or quantitative defects of dystrophin | MONDO_0016147 | |
| microcephalic primordial dwarfism due to RTTN deficiency | MONDO_0018764 | |
| SMARCA4-deficient sarcoma of thorax | MONDO_0018761 | |
| DeSanto-Shinawi syndrome | MONDO_0018760 | |
| cloacogenic carcinoma | MONDO_0004129 | |
| hyperamylasemia | MONDO_0006789 | |
| thyroiditis | MONDO_0004126 | |
| rectum leiomyoma | MONDO_0004125 |