All terms in MONDO
| Label | Id | Description |
|---|---|---|
| alexithymia | MONDO_0000661 | |
| defective phagocytic cell opsonization | MONDO_0024632 | |
| akinetopsia | MONDO_0000660 | |
| auditory agnosia | MONDO_0000667 | |
| associative visual agnosia | MONDO_0000666 | |
| visual agnosia | MONDO_0000685 | |
| apperceptive agnosia | MONDO_0000664 | |
| microphthalmia-brain atrophy syndrome | MONDO_0012638 | |
| hereditary spastic paraplegia 18 | MONDO_0012639 | |
| restless legs syndrome, susceptibility to, 6 | MONDO_0012636 | |
| COG1-congenital disorder of glycosylation | MONDO_0012637 | |
| familial reactive perforating collagenosis | MONDO_0009000 | |
| autosomal recessive limb-girdle muscular dystrophy type 2L | MONDO_0012652 | |
| persistent hyperplastic primary vitreous, autosomal dominant | MONDO_0012653 | |
| persistent hyperplastic primary vitreous | MONDO_0019631 | |
| Cernunnos-XLF deficiency | MONDO_0012650 | |
| spastic ataxia 2 | MONDO_0012651 | |
| lethal congenital contracture syndrome 3 | MONDO_0012656 | |
| Mungan syndrome | MONDO_0012657 | |
| atrial septal defect 4 | MONDO_0012654 |