All terms in MONDO
| Label | Id | Description |
|---|---|---|
| congenital afibrinogenemia | MONDO_0008737 | |
| familial dysfibrinogenemia | MONDO_0014452 | |
| peroxisome biogenesis disorder 2B | MONDO_0008736 | |
| non-classic presentation | MONDO_0100357 | |
| adrenocortical unresponsiveness to ACTH with postreceptor defect | MONDO_0008735 | |
| familial glucocorticoid deficiency | MONDO_0008733 | |
| adrenocortical carcinoma, hereditary | MONDO_0008734 | |
| adrenal cortex carcinoma | MONDO_0006639 | |
| adrenal hypoplasia, cytomegalic type | MONDO_0008732 | |
| X-linked adrenal hypoplasia congenita | MONDO_0010264 | |
| familial adrenal hypoplasia with absent pituitary luteinizing hormone | MONDO_0008731 | |
| 46,XY disorder of sex development | MONDO_0020040 | |
| congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency | MONDO_0008730 | |
| polyneuritis | MONDO_0021718 | |
| polyneuropathy | MONDO_0001824 | |
| neuritis | MONDO_0002122 | |
| pseudohypoparathyroidism type 2 | MONDO_0008749 | |
| pseudohypoparathyroidism | MONDO_0019992 | |
| Hermansky-Pudlak syndrome 1 | MONDO_0008748 | |
| Hermansky-Pudlak syndrome with pulmonary fibrosis | MONDO_0016501 |