All terms in MONDO
| Label | Id | Description |
|---|---|---|
| taurodontism, microdontia, and dens invaginatus | MONDO_0010740 | |
| thrombocytopenia 1 | MONDO_0010743 | |
| pentalogy of Cantrell | MONDO_0010742 | |
| chondrodysplasia | MONDO_0022723 | |
| obsolete chondrodysplasia lethal recessive | MONDO_0022725 | |
| MONDO_0022728 | MONDO_0022728 | |
| chondrodysplasia punctata with steroid sulfatase deficiency | MONDO_0022729 | |
| mosaic variegated aneuploidy syndrome 1 | MONDO_0009759 | |
| congenital stationary night blindness 1B | MONDO_0009758 | |
| obsolete chorea minor | MONDO_0022732 | |
| Niemann-Pick disease, type C1 | MONDO_0009757 | |
| choreoacanthocytosis amyotrophic | MONDO_0022733 | |
| spatial visualization, aptitude for | MONDO_0010734 | |
| Niemann-Pick disease type A | MONDO_0009756 | |
| hereditary spastic paraplegia 2 | MONDO_0010733 | |
| neutrophil actin dysfunction | MONDO_0009755 | |
| split hand-foot malformation 2 | MONDO_0010736 | |
| neutropenia, lethal congenital, with eosinophilia | MONDO_0009754 | |
| Kennedy disease | MONDO_0010735 | |
| obsolete neurovisceral storage disease with Curvilinear bodies | MONDO_0009753 |