All terms in MONDO
| Label | Id | Description |
|---|---|---|
| Jawad syndrome | MONDO_0009622 | |
| hemophilia A with vascular abnormality | MONDO_0010603 | |
| microcephaly-cervical spine fusion anomalies syndrome | MONDO_0009621 | |
| hernia, anterior diaphragmatic | MONDO_0010606 | |
| congenital diaphragmatic hernia | MONDO_0005711 | |
| Say-Barber-Miller syndrome | MONDO_0009620 | |
| hemopoietic proliferation | MONDO_0010605 | |
| Hhhh syndrome | MONDO_0010608 | |
| heterotaxy, visceral, 1, X-linked | MONDO_0010607 | |
| hypouricemia, familial renal, due to tubular hypersecretion | MONDO_0010620 | |
| hereditary renal hypouricemia | MONDO_0009071 | |
| recessive X-linked ichthyosis | MONDO_0010622 | |
| inherited ichthyosis | MONDO_0015947 | |
| sterol metabolism disorder | MONDO_0019256 | |
| CHILD syndrome | MONDO_0010621 | |
| X-linked chondrodysplasia punctata | MONDO_0010556 | |
| brachydactyly small stature face anomalies | MONDO_0022602 | |
| brachydactyly tibial hypoplasia | MONDO_0022603 | |
| food allergy | MONDO_0700226 | |
| obsolete brachymetapody anodontia hypotrichosis albinoidism | MONDO_0022605 |