All terms in MONDO
| Label | Id | Description |
|---|---|---|
| osteogenesis imperfecta type 14 | MONDO_0014029 | |
| gliomatosis cerebri | MONDO_0016683 | |
| hereditary spastic paraplegia 55 | MONDO_0014020 | |
| c12orf65-related combined oxidative phosphorylation defect | MONDO_0044655 | |
| anaplastic astrocytoma | MONDO_0016684 | |
| hereditary spastic paraplegia 43 | MONDO_0014024 | |
| congenital muscular dystrophy with intellectual disability and severe epilepsy | MONDO_0014023 | |
| disorder of multiple glycosylation | MONDO_0017749 | |
| muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 | MONDO_0014022 | |
| gliosarcoma | MONDO_0016681 | |
| brain glioblastoma | MONDO_0002501 | |
| giant cell glioblastoma | MONDO_0016682 | |
| familial episodic pain syndrome with predominantly upper body involvement | MONDO_0014021 | |
| alcohol abuse | MONDO_0002046 | |
| substance abuse | MONDO_0002491 | |
| pulmonary systemic sclerosis | MONDO_0002047 | |
| thrombocytopenia due to immune destruction | MONDO_0002048 | |
| thrombocytopenia | MONDO_0002049 | |
| mechanical ectropion | MONDO_0002042 | |
| ectropion | MONDO_0002043 |