All terms in MONDO
| Label | Id | Description |
|---|---|---|
| autosomal dominant cataract | MONDO_0022672 | |
| autosomal dominant non-nuclear cataract | MONDO_0022673 | |
| congenital isolated hyperinsulinism | MONDO_0019010 | |
| islet cell adenomatosis | MONDO_0007834 | |
| cataract skeletal anomalies | MONDO_0022675 | |
| obsolete cataract - glaucoma | MONDO_0022676 | |
| Duchenne muscular dystrophy | MONDO_0010679 | |
| dilated cardiomyopathy 3B | MONDO_0010542 | |
| Achoo syndrome | MONDO_0007038 | |
| obsolete rare neurologic disease with psychiatric involvement | MONDO_0020016 | |
| muscular dystrophy, progressive Pectorodorsal | MONDO_0010678 | |
| neurofibromatosis type 2 | MONDO_0007039 | |
| obsolete rare circulatory system disease | MONDO_0020015 | |
| action myoclonus-renal failure syndrome | MONDO_0009699 | |
| obsolete rare disease with odontological manifestation | MONDO_0020014 | |
| Achard syndrome | MONDO_0007036 | |
| achondroplasia | MONDO_0007037 | |
| obsolete rare odontologic disease | MONDO_0020013 | |
| Lafora disease | MONDO_0009697 | |
| obsolete systemic or rheumatic disease | MONDO_0020012 |