All terms in MONDO
| Label | Id | Description |
|---|---|---|
| Binder syndrome | MONDO_0007953 | |
| obsolete May-Hegglin anomaly | MONDO_0007954 | |
| masticatory muscles, hypertrophy of | MONDO_0007951 | |
| maxillofacial dysostosis | MONDO_0007952 | |
| CEBALID syndrome | MONDO_0032908 | |
| 49,XXXXY syndrome | MONDO_0019929 | |
| mitochondrial complex 3 deficiency, nuclear type 10 | MONDO_0032909 | |
| spastic paraplegia 82, autosomal recessive | MONDO_0032906 | |
| lymphatic malformation 8 | MONDO_0032907 | |
| rippling muscle disease 2 | MONDO_0019947 | |
| zebra body myopathy | MONDO_0019949 | |
| Eisenmenger syndrome | MONDO_0019944 | |
| hereditary continuous muscle fiber activity | MONDO_0019943 | |
| ligneous conjunctivitis | MONDO_0019946 | |
| solar urticaria | MONDO_0019945 | |
| hypertrichosis-acromegaloid facial appearance syndrome | MONDO_0019940 | |
| vertebral joint disorder | MONDO_0037847 | |
| spondylitis | MONDO_0003937 | |
| melanoma tumor antigen Gp90 | MONDO_0007968 | |
| spinal fracture | MONDO_0005309 |