| Label | Id | |
|---|---|---|
| irid 2 | http://purl.obolibrary.org/obo/MONDO_0007662 | |
| iridogoniodysgenesis, type 2 | 7662 | |
| iridogoniodysgenesis caused by mutation in PITX2 | 7662 | |
| iridogoniodysgenesis, type 2; IRID2 | http://purl.obolibrary.org/obo/MONDO_0007662 | |
| anterior segment dysgenesis 4 | 7662 | |
| miscellaneous movement disorder due to genetic neurodegenerative disease | 17662 | |
| anterior segment dysgenesis 4; ASGD4 | http://purl.obolibrary.org/obo/MONDO_0007662 | |
| battaglia neri syndrome | C537662 | |
| iris hypoplasia with early-onset glaucoma, autosomal dominant | 7662 |