| Label | Id | |
|---|---|---|
| CPHD2 | 9878 | |
| dup(3)(q26) | 19878 | |
| dup(3q) syndrome | 19878 | |
| trisomy 3q26 | 19878 | |
| Hanhart dwarfism | 9878 | |
| achondrogenesis syndrome | C579878 | |
| pituitary dwarfism 3 | 9878 | |
| Cornelia de Lange-like syndrome | 19878 | |
| pituitary hormone deficiency, combined, 2 | 9878 | |
| pituitary hormone deficiency, combined, 2; CPHD2 | http://purl.obolibrary.org/obo/MONDO_0009878 | |
| pituitary hormone deficiency, combined, type 2 | 9878 | |
| combined pituitary hormone deficiencies, genetic form caused by mutation in PROP1 | 9878 | |
| PROP1 combined pituitary hormone deficiencies, genetic form | 9878 | |
| 3q26 microduplication syndrome | 19878 | |
| ateliotic dwarfism with hypogonadism | 9878 |